An inspection was conducted on three orders of hangbags from a factory in Guangzhou, China. Several defects were found, including stuck zippers, open seams, and untrimmed threads. Samples from orders 10878 and 18678 failed the inspection due to defect rates exceeding the allowed quality limits. The factory agreed to rework the defective items from order 10878. Overall, the inspection results for the three orders were rejected.
This document provides a warehouse design and layout project for storing 20 different products across 3 categories. It includes calculations for space needed in receiving, shipping, picking, sorting, and bulk storage areas. The receiving area is designed to hold one day of incoming goods. The shipping area is designed to hold 1.5 days of goods. The picking area holds one full day of product for each SKU. The sorting area holds one hour of goods. Bulk storage holds the calculated safety stock levels. The total proposed warehouse area is 74,600 square feet based on the layout and space calculations provided.
This document provides guidance on final random inspection procedures and reporting. It defines key terms like quality, defects, and sampling plans. It outlines the inspection process, including reviewing technical documents, carton selection, checking packaging/markings, measurements, weights, visual quality, functions, and barcodes. Inspectors are to draw samples, record any non-conformities, and provide a detailed report on the inspection results and environment.
The document provides guidance on conducting Annual Product Reviews (APRs), including:
- APRs are required annually for commercial products to verify consistency, assess trends, determine specification/process changes, and evaluate revalidation needs.
- APRs must include review of batches manufactured, deviations, complaints, recalls, changes, specifications, validation status, and trend analyses. Additional requirements may apply from local regulations.
- The review concludes if the product consistently meets quality attributes and necessary corrective actions. APRs communicate between manufacturing, quality, and regulatory to enable quality improvement.
A technical writeup on PERFORMANCE of a CARTON.
Explains the Importance of Box Compression Test and breaks myths about the relevance of Bursting Strength Test
We all have a general understanding of how inventory counting works, but do we really know the best practices and why they are so important? This presentation discusses that further
This document provides a warehouse design and layout project for storing 20 different products across 3 categories. It includes calculations for space needed in receiving, shipping, picking, sorting, and bulk storage areas. The receiving area is designed to hold one day of incoming goods. The shipping area is designed to hold 1.5 days of goods. The picking area holds one full day of product for each SKU. The sorting area holds one hour of goods. Bulk storage holds the calculated safety stock levels. The total proposed warehouse area is 74,600 square feet based on the layout and space calculations provided.
This document provides guidance on final random inspection procedures and reporting. It defines key terms like quality, defects, and sampling plans. It outlines the inspection process, including reviewing technical documents, carton selection, checking packaging/markings, measurements, weights, visual quality, functions, and barcodes. Inspectors are to draw samples, record any non-conformities, and provide a detailed report on the inspection results and environment.
The document provides guidance on conducting Annual Product Reviews (APRs), including:
- APRs are required annually for commercial products to verify consistency, assess trends, determine specification/process changes, and evaluate revalidation needs.
- APRs must include review of batches manufactured, deviations, complaints, recalls, changes, specifications, validation status, and trend analyses. Additional requirements may apply from local regulations.
- The review concludes if the product consistently meets quality attributes and necessary corrective actions. APRs communicate between manufacturing, quality, and regulatory to enable quality improvement.
A technical writeup on PERFORMANCE of a CARTON.
Explains the Importance of Box Compression Test and breaks myths about the relevance of Bursting Strength Test
We all have a general understanding of how inventory counting works, but do we really know the best practices and why they are so important? This presentation discusses that further
validation of blister packaging machineNilesh Utpure
The document discusses validation of packaging machines. It outlines the objectives, importance, and responsibilities of process validation. Validation establishes that a machine meets installation, operational, and performance qualification requirements. The document describes user requirement specifications that cover mandatory parts to guarantee final product quality and compliance. It details the scope, steps in the machine's lifecycle, types of packaging machines, their detailed assembly, key parameters, and the validation SOP.
This document discusses packaging material standards for exporting products. It covers several key points:
1. Packaging design should be based on consumer needs and protect the product based on its intended use. Regulations vary by country.
2. Packaging materials must be food grade for food products and maintain product properties. They should not contaminate or affect the product.
3. Export packaging requires identifying information, instructions, and compliance with importing country regulations. Proper labeling, markings, and certifications are needed.
4. Packaging examples are provided for various fruits and vegetables being exported, specifying materials, dimensions, and other requirements. Standards ensure safe and effective packaging for international trade.
This document appears to be an inspection report form used by inspectors from the World Health Organization (WHO) to inspect pharmaceutical manufacturing firms and ensure compliance with Good Manufacturing Practices (GMP). The form includes sections to record details of the firm, personnel, facilities, equipment, materials, documentation, production processes, and compliance with GMP standards. Inspectors would use this form to systematically evaluate all aspects of the facility and operations during an inspection.
Unit 02 chapter 05 documentation systems documents and record keepingDominic Parry
This document discusses documentation and record keeping requirements for quality management systems. It covers the key principles of documentation including accuracy, integrity and availability. It describes the types of documents and records required such as specifications, manufacturing instructions, certificates and reports. The document provides details on EU GMP chapter 4 requirements for documentation practices, document control, record retention and approval. It emphasizes that a documentation system is essential to meet regulatory standards and continual improvement.
L&T Valves - Role of NDT in Valve IndustriesBabu Kuriakose
The document discusses the role of non-destructive testing (NDT) in valve industries. It provides an overview of L&T Valves Limited, including its facilities, certifications, and customers. It then discusses LTVL's NDT journey, current NDT practices, challenges, and improvements made. Specific topics covered include personnel qualifications, NDT processes, validation, customer demands vs LTVL practices, case studies of NDT failures, and interpretations of ASME standards taken up by LTVL.
The document describes quality control and warehousing procedures. It includes flow charts showing the inspection process for materials from suppliers through various production stages to final packaging. Samples are sent to certified labs for chemical testing. Materials are inspected according to checklists and drawings before final packaging or being sent back. Standards used include Danish, ASTM, and AISI. Quality norms specify dimensions, fitment, finishing, and materials. Warehousing involves batch numbering, first in first out storage, packing materials, segregated and labeled storage, and labeling equipment.
Product Quality Reviews (PQRs) are conducted annually to review manufacturing processes, specifications, trends, and identify improvements for pharmaceutical products. PQRs can be done on individual products, grouped products, or through exception reviews. The objective is to verify consistency, specifications, identify trends, and improvements. PQRs provide information on processes, quality requirements, and release decisions. Outcomes are used to identify continuous quality improvements through action plans. Manufacturers are responsible for preparing review data and lists, while reviews consider starting materials, specifications, failures, deviations, changes, variations, stability, complaints, and contractual arrangements.
Handling of Customer Complaint_Dr.A.AmsavelDr. Amsavel A
Reference Guideline
Definitions
GMP Requirement: 21 CFR § 211.198 and ICH Q7
Procedure for Handling of Complaints
Complaint Investigation
Remedial action and CAPA
Report preparation
Response to customer
Verification of CAPA effectiveness
Review of Complaints
According to US FDA it is illustrated here that,
A recall is a method of removing or correcting products that are in violation of laws administered by the Drug Regulatory Authority.
Recall is a voluntary action that takes place because manufacturers and distributors carry out their responsibility to protect the public health and well-being from products that present a risk of injury or gross deception or are otherwise defective.
21 CFR 7 provides guidance so that responsible firms may conduct an effective recall.
Process Flow Chart of Garments Manufacturing | Sequence of Garments Production Process/ Process Flow Chart of Garments Manufacturing | Sequence of Garments Production Process/ Knit Garments factory
Garments Manufacturing Flow chart
How to make garments ?
RMG Flow Chart
Grain Silo Installation Checklist consolidates most of Installation checks that one should perform while doing installation of Grain Silos so that nothing goes wrong after the installations
This document outlines procedures for handling deviations from standard operating procedures in a cGMP environment. It defines deviations as planned or unplanned activities that differ from specified procedures. Planned deviations are deliberate temporary changes that don't affect quality, while unplanned deviations result from failures or errors. The procedures describe rules for documenting deviations, evaluating their quality impact, approving corrective actions, and filing reports. Deviations are assigned a control number and approved by quality assurance to ensure proper handling. Repeated deviations must be investigated and corrective actions taken to prevent reoccurrences.
This document outlines the process validation plan for a solid dosage anti-tuberculosis drug. It begins with an introduction and outline. It then discusses the stages of process validation, literature review, and plan of work. The document describes the manufacturing process and identifies critical and non-critical process parameters. It discusses sampling plans, statistical tools for analysis, and key references. The overall aim is to assure consistent quality and reduce defects through process validation.
This document outlines the standard operating procedures for purchasing at Al Shifa Hospital Pvt. Ltd. It details the 22 steps in the purchasing process from raising a purchase request to disposing of damaged or expired items. Key responsibilities include the purchase assistant collecting quotations, purchase manager preparing purchase orders, and store incharge receiving, storing, and maintaining stock. Suppliers are evaluated every six months based on quality and delivery ratings to determine inclusion on the approved supplier list.
Common GMP errors include not following safety procedures, improper cleaning practices, and incomplete documentation. Some specific mistakes are failing to wear proper protective equipment, using unapproved materials, and making undocumented changes to records. These errors can be avoided by always following safety rules, keeping accurate records using indelible ink, ensuring equipment is calibrated, and not bringing food or drinks into work areas. Vigilance is important to prevent contamination and ensure accurate documentation.
The document outlines standard operating procedures for alarmed garments at Asian Group Properties in Chittagong, Bangladesh. It details that (1) needle detector operators and production supervisors are responsible for ensuring garments pass through metal detectors without needle fragments, (2) garments that do not pass must be searched by handheld metal detectors to identify contaminated areas, and (3) any contaminated parts found must be removed and properly recorded, with the garment rechecked before reuse.
The document outlines statutory guidelines regarding pre-packaged commodities under the Legal Metrology Act of 2009. It discusses various rules for declarations that must be made on pre-packaged goods, including the name and address of the manufacturer/packer, generic name of product, quantity, dimensions, expiration dates and maximum retail price. Specific rules are provided for retail goods, goods manufactured and packed by a third party, and imported goods. Proper labeling helps ensure accurate information is provided to consumers of pre-packaged commodities.
This quality assurance plan outlines the procedures for fabricating and inspecting pipes at a shop for a client's project. It describes 11 manufacturing stages including receiving raw materials, welding, gauging, leakage testing, dimensional checks, and certification. Control checks and reference documents are provided for each stage, along with the manner of recording inspections. The plan aims to ensure pipes are manufactured according to specifications.
This document outlines various verification, investigation, and quality control services provided by Chinabizcheckup.com to assist foreign companies doing business in China. It lists service categories including verification, purchasing agent services, sourcing suppliers, and quality control. For each category, it provides descriptions of specific services and the charges in US dollars to complete them, ranging from $180 to $250 per day plus travel costs. It notes services can be customized and final costs may vary depending on the project.
validation of blister packaging machineNilesh Utpure
The document discusses validation of packaging machines. It outlines the objectives, importance, and responsibilities of process validation. Validation establishes that a machine meets installation, operational, and performance qualification requirements. The document describes user requirement specifications that cover mandatory parts to guarantee final product quality and compliance. It details the scope, steps in the machine's lifecycle, types of packaging machines, their detailed assembly, key parameters, and the validation SOP.
This document discusses packaging material standards for exporting products. It covers several key points:
1. Packaging design should be based on consumer needs and protect the product based on its intended use. Regulations vary by country.
2. Packaging materials must be food grade for food products and maintain product properties. They should not contaminate or affect the product.
3. Export packaging requires identifying information, instructions, and compliance with importing country regulations. Proper labeling, markings, and certifications are needed.
4. Packaging examples are provided for various fruits and vegetables being exported, specifying materials, dimensions, and other requirements. Standards ensure safe and effective packaging for international trade.
This document appears to be an inspection report form used by inspectors from the World Health Organization (WHO) to inspect pharmaceutical manufacturing firms and ensure compliance with Good Manufacturing Practices (GMP). The form includes sections to record details of the firm, personnel, facilities, equipment, materials, documentation, production processes, and compliance with GMP standards. Inspectors would use this form to systematically evaluate all aspects of the facility and operations during an inspection.
Unit 02 chapter 05 documentation systems documents and record keepingDominic Parry
This document discusses documentation and record keeping requirements for quality management systems. It covers the key principles of documentation including accuracy, integrity and availability. It describes the types of documents and records required such as specifications, manufacturing instructions, certificates and reports. The document provides details on EU GMP chapter 4 requirements for documentation practices, document control, record retention and approval. It emphasizes that a documentation system is essential to meet regulatory standards and continual improvement.
L&T Valves - Role of NDT in Valve IndustriesBabu Kuriakose
The document discusses the role of non-destructive testing (NDT) in valve industries. It provides an overview of L&T Valves Limited, including its facilities, certifications, and customers. It then discusses LTVL's NDT journey, current NDT practices, challenges, and improvements made. Specific topics covered include personnel qualifications, NDT processes, validation, customer demands vs LTVL practices, case studies of NDT failures, and interpretations of ASME standards taken up by LTVL.
The document describes quality control and warehousing procedures. It includes flow charts showing the inspection process for materials from suppliers through various production stages to final packaging. Samples are sent to certified labs for chemical testing. Materials are inspected according to checklists and drawings before final packaging or being sent back. Standards used include Danish, ASTM, and AISI. Quality norms specify dimensions, fitment, finishing, and materials. Warehousing involves batch numbering, first in first out storage, packing materials, segregated and labeled storage, and labeling equipment.
Product Quality Reviews (PQRs) are conducted annually to review manufacturing processes, specifications, trends, and identify improvements for pharmaceutical products. PQRs can be done on individual products, grouped products, or through exception reviews. The objective is to verify consistency, specifications, identify trends, and improvements. PQRs provide information on processes, quality requirements, and release decisions. Outcomes are used to identify continuous quality improvements through action plans. Manufacturers are responsible for preparing review data and lists, while reviews consider starting materials, specifications, failures, deviations, changes, variations, stability, complaints, and contractual arrangements.
Handling of Customer Complaint_Dr.A.AmsavelDr. Amsavel A
Reference Guideline
Definitions
GMP Requirement: 21 CFR § 211.198 and ICH Q7
Procedure for Handling of Complaints
Complaint Investigation
Remedial action and CAPA
Report preparation
Response to customer
Verification of CAPA effectiveness
Review of Complaints
According to US FDA it is illustrated here that,
A recall is a method of removing or correcting products that are in violation of laws administered by the Drug Regulatory Authority.
Recall is a voluntary action that takes place because manufacturers and distributors carry out their responsibility to protect the public health and well-being from products that present a risk of injury or gross deception or are otherwise defective.
21 CFR 7 provides guidance so that responsible firms may conduct an effective recall.
Process Flow Chart of Garments Manufacturing | Sequence of Garments Production Process/ Process Flow Chart of Garments Manufacturing | Sequence of Garments Production Process/ Knit Garments factory
Garments Manufacturing Flow chart
How to make garments ?
RMG Flow Chart
Grain Silo Installation Checklist consolidates most of Installation checks that one should perform while doing installation of Grain Silos so that nothing goes wrong after the installations
This document outlines procedures for handling deviations from standard operating procedures in a cGMP environment. It defines deviations as planned or unplanned activities that differ from specified procedures. Planned deviations are deliberate temporary changes that don't affect quality, while unplanned deviations result from failures or errors. The procedures describe rules for documenting deviations, evaluating their quality impact, approving corrective actions, and filing reports. Deviations are assigned a control number and approved by quality assurance to ensure proper handling. Repeated deviations must be investigated and corrective actions taken to prevent reoccurrences.
This document outlines the process validation plan for a solid dosage anti-tuberculosis drug. It begins with an introduction and outline. It then discusses the stages of process validation, literature review, and plan of work. The document describes the manufacturing process and identifies critical and non-critical process parameters. It discusses sampling plans, statistical tools for analysis, and key references. The overall aim is to assure consistent quality and reduce defects through process validation.
This document outlines the standard operating procedures for purchasing at Al Shifa Hospital Pvt. Ltd. It details the 22 steps in the purchasing process from raising a purchase request to disposing of damaged or expired items. Key responsibilities include the purchase assistant collecting quotations, purchase manager preparing purchase orders, and store incharge receiving, storing, and maintaining stock. Suppliers are evaluated every six months based on quality and delivery ratings to determine inclusion on the approved supplier list.
Common GMP errors include not following safety procedures, improper cleaning practices, and incomplete documentation. Some specific mistakes are failing to wear proper protective equipment, using unapproved materials, and making undocumented changes to records. These errors can be avoided by always following safety rules, keeping accurate records using indelible ink, ensuring equipment is calibrated, and not bringing food or drinks into work areas. Vigilance is important to prevent contamination and ensure accurate documentation.
The document outlines standard operating procedures for alarmed garments at Asian Group Properties in Chittagong, Bangladesh. It details that (1) needle detector operators and production supervisors are responsible for ensuring garments pass through metal detectors without needle fragments, (2) garments that do not pass must be searched by handheld metal detectors to identify contaminated areas, and (3) any contaminated parts found must be removed and properly recorded, with the garment rechecked before reuse.
The document outlines statutory guidelines regarding pre-packaged commodities under the Legal Metrology Act of 2009. It discusses various rules for declarations that must be made on pre-packaged goods, including the name and address of the manufacturer/packer, generic name of product, quantity, dimensions, expiration dates and maximum retail price. Specific rules are provided for retail goods, goods manufactured and packed by a third party, and imported goods. Proper labeling helps ensure accurate information is provided to consumers of pre-packaged commodities.
This quality assurance plan outlines the procedures for fabricating and inspecting pipes at a shop for a client's project. It describes 11 manufacturing stages including receiving raw materials, welding, gauging, leakage testing, dimensional checks, and certification. Control checks and reference documents are provided for each stage, along with the manner of recording inspections. The plan aims to ensure pipes are manufactured according to specifications.
This document outlines various verification, investigation, and quality control services provided by Chinabizcheckup.com to assist foreign companies doing business in China. It lists service categories including verification, purchasing agent services, sourcing suppliers, and quality control. For each category, it provides descriptions of specific services and the charges in US dollars to complete them, ranging from $180 to $250 per day plus travel costs. It notes services can be customized and final costs may vary depending on the project.
An inspection was conducted of a shipment of 5000 pens from a factory in Tonglu, Zhejiang, China. The inspection found that the quantity, product description, workmanship, testing, data measurement, and packaging all met requirements, with only minor defects found. A sample of 315 pens was inspected and 1 pen had a scratch, 4 had black dots, and 1 had a rusty spot. The inspection report included photos documenting the packaging, product, and defects. The overall inspection result was passed.
Inspection report from Mirrored Cabidor on July 12th,2016河 黄
An inspection was conducted of a mirrored cabidor product on July 12, 2016. 511 units were available and sampled, with 1 minor defect found of exposed nails in holes and 6 minor defects found of dirty marks on surfaces. Pictures show the defects and details of the product, packaging, and inspection measurements. The factory workers reworked the defective units.
1) The document discusses the design process for unique jewelry, noting that designers first sketch ideas on paper before setting gems.
2) It provides examples of unique jewelry designs commissioned from Cartier using rare diamonds and gemstones, with complex designs set in platinum.
3) A particular design from the 1930s is highlighted, using small sapphires set in a square mesh platinum surface.
1. CHINABIZCHECKUP-Your camera in the factory
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Report No.: SZ160727
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Chinabizcheckup
INSPECTION RESULT SUMMARY
Category Conform Not Conform Pending
1.Quantity √
2.Workmanship √
3.Style, Color & Documentation √
4.Field Test & Measurement √
5.Shipping Mark & Packaging √
OVERALL CONCLUSION Rejected
Both colors of red and beige items from 10878 went beyond AQL limted.so factory has agreed our
advice to rework two items.please be noted!
INSPECTION DETAILS
Item No Order Qty(carton) Order Qty(pcs) Sample size(pcs)
10878 35+20+20 700+400+400 80/50/50
PRE-SHIPMENT INSPECTION REPORT Report No.: SZ160727
INSPECTION INFORMATION
Factory Guangzhou Yusheng Leather Factory
Inspector Evan Inspection Standard MIL-STD-105E
P.O. No. #4135 #4315 Sampling Plan Randomly inspect
Product Name Hangbags Sampling Level II levels
Inspection Date July 27th
,2016 Sample Size To refer to the order
Inspection Location Huandu District,Guangzhou AQL Major:2.5 Minor:4.0
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18678 30+20 600+400 80/50
18679 33+20 500+300 50/50
Defects Description
Item Defect description Critical Major Minor
10878
Zipper head is stuck 0 5 12
Open seam 0 6 10
Untrimmed thread residue 0 0 6
18678
Mixed color 0 1 1
Open seam 0 0 1
Untrimmed thread residue 0 0 4
18679 Poor sewing 0 0 1
Defect pictures from 10878
The zipper head is got stuck when it’s moved The zipper head is got stuck when it’s moved
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Open seam Open seam
Open seam Open seam
Open seam Open seam
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Open seam Open seam
Untrimmed thread residue Untrimmed thread residue
Defect pictures from 18678
Mixed color on the leather Mixed color on the leather
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Open seam Untrimmed thread residue
Untrimmed thread residue Untrimmed thread residue
Untrimmed thread residue Untrimmed thread residue
Defect pictures from 18679
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Poor sewing Untrimmed thread residue
Pack&Product Information for 10878
Finished goods Carton box view
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Front mark(black) Front mark (beige)
Front mark(red) Side mark
Side mark(black) Side mark(beige)
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Side mark(red) Opening carton box to view
Fluting paper with seven layers Opening carton box to view
Poly bag view Pack view
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Pack view Poly bag view
Pack view Pack view
Poly bag view Three color of the items view
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Left side of item is sample and right side of item is bulk
production
Left side of item is sample and right side of item is bulk
production
Three color of the items view Logo view
Product view in details Product view in details
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Product view in details Product view in details
Hangtag view Hangtag view
Bar code scanned Bar code scanned
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Hangtag view Hangtag view
Bar code scanned Bar code scanned
Hangtag view Hangtag view
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Bar code scanned Bar code scanned
Three colors of the items view Product view in details
Product view in details Product view in details
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Product view in details Product view in details
Product view in details Product view in details
Product view in details Product view in details
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Product view in details Product view in details
Product view in details Product view in details
Product view in details Fabric label with bar code
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Bar code scanned Fabric label with bar code
Bar code scanned Fabric label with bar code
Bar code scanned Non-woven bag view
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Logo view Non-woven bag view
Product view Product view
Nil
Product view Nil
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Measurement Date from 10878
Gross weight check Gross weight show
Gross weight check Gross weight show
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Gross weight check Gross weight show
Size measurement Size measurement
Size measurement Size measurement
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Size measurement Size measurement
Size measurement Size measurement
Size measurement Size measurement
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Size measurement Size measurement
Size measurement Size measurement
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Size measurement Single net weight show
Single net weight show Single net weight show
Pack and Product Information from 18678
Finished goods Finished goods
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Carton box view Front mark(camel)
Side mark (camel) Front mark(black)
Front mark(black) Side mark(black)
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Pack view Fluting paper with seven layers
Pack view Poly bag view
Poly bag view Two items views
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The approved color sample is matched with the bulk production The approved color sample is matched with the bulk production
Products view in details Product view in details
Product view in details Product view in details
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Product view in details Product view in details
Product view in details Product view in details
Product view in details Product view in details
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Report No.: SZ160727
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Product view in details Product view in details
Product view in details Product view in details
Product view in details Products view in details
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Product view in details Product view in details
Product view in details Product view in details
Product view in details Hangtag view
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Hangtag view Bar code scanned
Bar code scanned Hangtag view
Hangtag view Bar code scanned
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Bar code scanned Product view in details
Products view in details Products view in details
Product view in details Product view in details
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Product view in details Product view in details
Product view in details Product view in details
Product view in details Product view in details
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Product view in details Product view in details
Product view in details Product view in details
Product view in details Product view in details
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Product view in details Product view in details
Product view in details Product view in details
Product view in details Product view in details
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Product view in details Product view in details
Product view in details Product view in details
Product view in details Fabric label view
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Product view in details Products view in details
Product view Product view
Measurement Date from 18678
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Size measurement Size measurement
Size measurement Size measurement
Size measurement Size measurement
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Gross weight check Gross weight show
Gross weight check Gross weight show
Size measurement Size measurement
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Size measurement Size measurement
Size measurement Size measurement
Size measurement Size measurement
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Size measurement Size measurement
Size measurement Size measurement
Single net weight show Single net weight show
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Pack and Product Information from 18679
Finished goods Finished goods
Sid mark(black) Side mark(black)
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Front mark(camel) Side mark(camel)
Pack view Fluting paper with seven layers
Pack view Pack view
42. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 42 -
Pack view Two items view
Poly bag view Poly bag view
Products view in details Product view in details
43. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 43 -
Product view in details Hangtag view
Hangtag view Bar code scanned
Bar code scanned Product view in details
44. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 44 -
Product view in details Hangtag view
Hangtag view Bar code scanned
Bar code scanned Products view in details
45. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 45 -
Product view in details Product view in details
Product view in details Product view in details
Product view in details Product view in details
46. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 46 -
Products view in details Products view in details
Products view in details Products view in details
Products view in details Product view in details
47. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 47 -
Product view in details Product view in details
Product view in details Product view in details
Product view in details Product view in details
48. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 48 -
Product view in details Product view in details
Product view in details Product view in details
Product view in details Product view in details
49. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 49 -
Product view in details Fabric label view
Product view in details Product view in details
Product view in details Product view in details
50. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 50 -
Products view in details Product view in details
Products view in details Product view in details
Product view in details Product view in details
51. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 51 -
Product view in details Product view in details
Product view in details Product view in details
Product view in details Product view in details
52. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 52 -
Product view in details Product view in details
Product view in details Product view in details
Product view in details Product view in details
53. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 53 -
Product view in details Products view in details
Product view in details Products view in details
Products view in details Non-woven bag view
54. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 54 -
Non-woven bag view Product view
Product view Product view
Product view Product view
55. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 55 -
Measurement Date from 18679
Size measurement Size measurement
Size measurement Size measurement
Size measurement Size measurement
56. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 56 -
Gross weight check Gross weight show
Gross weight check Gross weight show
Single net weigh show Single net weight show
57. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 57 -
Size measurement Size measurement
Size measurement Size measurement
Size measurement Size measurement
58. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 58 -
Size measurement Size measurement
Size measurement Size measurement
Size measurement Size measurement
59. CHINABIZCHECKUP-Your camera in the factory
www.chinabizcheckup.com
Report No.: SZ160727
- 59 -
Nil
Size measurement Nil
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