Title Page
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A. Factory/Organization Information
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Date of Information
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Location
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Area
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Total Staff in factory
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Total Office Staff
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Total Worker
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Main Customer
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Product Type
Quality Management System
1.Quality Manual
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1.1 Update Quality Manual Available
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1.2 Regularly Revised
2. Mission, Vision, Goal, Policy & Objectives
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2.1 Organizational Mission & Vision
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2.2 Organizational Goals
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2.3 Quality Policy & Procedure
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2.4 Quality Objectives
3.Documents Control
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3.1 Master list of Document with establish date & Revisions.
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3.2 Customer's document are controlled
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3.3 External Documents are available
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3 .4 Document change is applied & effective
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3.5 Document change system controlled using IT system
Planning & Management Review
1.Production Planning & Control
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1.1 Production Planning System[any software]
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1. 2 Pro duction Planning data match with T&A and workstation.
2. P.P. Meeting
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2.1 Tech. Pack file organized. (All documents are available for specific style of buyers)
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2.2 Size set sample report
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2.3 Product conformance record
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2.4 Record of PPM copy with sign and seal.
3. Management Review Meeting
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3.1 MRM Policy, Procedure & Report
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3.2 Corrective & Preventive Actions
Resources
1. Human Resource (Men)
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1.1 Organizational Organogram & Job Description.
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1.2 Training Record & Communication
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1.3 Interview Record (Policy & Process)
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1.4 Skill Matrix
2. Machine
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2.1 Total Machine List (Running, Idle and Out dated)
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2.2 Machine calibration Record (In-house & 3rd. party both)
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2.3 Machine Maintenance Policy & Procedure
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2.4 Machine Maintenance Plan, Schedule & Record
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2.5 Working Instruction available for machine
3. Materials
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3.1 List of materials (raw materials o fproduct & any other materials)
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3.2 Material Receiving, Storing & Issuing system
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3.2.1 Use kanban/FIFO for receiving and separate receiving area
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3.2.2 Storing system (ERP or Manual) and capacity (sufficient) check
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3.2.3 Special materials storage condition
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3.3 Raw Materials Inspection System with Visible instruction (Countable & with Visible instruction (Countable &
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3.4 Raw Materials testing (in-house or 3rd party) Report
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3.5 Dedicated Qualified Lab Technician are available
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3.6 Qualified Inspector available
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3.7 Proper light source are available
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3.8 Inspection area are separated from workstation
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3.9 non-conformity items are separated or not (check with record)
4.Mother of Nature (Environment)
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4.1 Overall environment for worker
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4.2 Housekeeping system (5S)
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4.3 Environment for Stakeholder, Customer & Supplier comment & Feedback (Use any complain box)
Manufacturing
1. Cutting
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1.1 Fabric Relaxation (Separate area, Use palate, Work instruction, Qualified person & Record)
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1.2 Fabric Lay & Spreading (Area, Use Spreading machine or manpower, Work Instruction & Report)
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1.3 Pattern & Marker Check
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- CAD & Pattern
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- Pattern adjustment system (grain line)
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- Area and CAD software with quailed person.
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1.4 Cut pane l Checking SOP (TMB & 100 % check) & Work Instruction are available
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1.5 Cutting part replacement SOP with separate area & qualified person
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1.6 Cutting replacement work instruction are available.
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1.7 Cutting parts replacement fabric storing as per SOP (Roll to roll or Lot to lot)
2. Print & Embroidery
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2.1 Print & Embroider SOP
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2.2 Work Instruction & checking area with adequate light sources.
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2.3 Checking procedure & Record
3. Fusing
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3.1 Fusing Data Sheet is available
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3.2 Work Instruction, Fusing SOP, Dedicated qualified person & Record are available with verification
4.Sewing
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4.1 Sewing layout & Machine adjustment record.
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4.2 Traffic Light System
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4.3 In process Checking System
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4.4 BIN Card & Mock Up for critical operations.
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4.5 Process Risk & Opportunity assessment
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4.6 How many tools are using for
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4.7 Defect Control Procedure
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4.8 Traceability of Production
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4.9 Oil Control Report is available
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4.10 Bingo Card is every MC
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4.11 Trim Card is available in sewing line
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4.12 Approved sample is in Sewing line
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4.13 Output QI report is available
5. Finishing
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5.1 Marking for Pressing, Visible work instruction and Operator must know how to use equipment & template.
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5.2 Visible work instruction about packing method.
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5.3 Pre-final & Final Report with measurement
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5.4 Defect Control List
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5.5 Corrective & Preventive action plan
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5.6 Independent Qualified QA team
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5.7 Visual Product and measurement Check like 32 pcs
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5.8 Product Re-call Procedure & Record
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5.9 Customer complaint Procedure & Record
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5.10 Final Product storing area use palate and maintain procedure
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5.11 Leftover procedure & record
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5.12 Final Product Disposal policy & Procedure
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5.13 Product disposal Record
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5.14 Output QI report is available
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5.15 Dry room report is available
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5.16 CTPAT area free for Sharp Tool
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5.17 Metal free zone is available
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5.18 Is iron SOP is available
Product Safety & Integrity
1. Button & Label Control
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1.1 Button Control Procedure properly maintain and record are verified.
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1.2 Label Control Procedure properly maintain and record are verified.
2. Machine Attachment Control
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2.1 Machine Attachment regularly check and maintain data sheet
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2.2 Machine Attachment control regularly and recorded.
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2.3 Machine oil level is ok.
3. Needle & Sharp metal Control
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3.1 Needle & Sharp metal control policy & procedure.
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3.2 Needle management system (receiving, storing, issuing) properly maintain.
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3.3 Broken Needle Procedure are followed properly.
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3.4 Qualified Needle man are available
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3.5 List of Sharp metal
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3.6 Sharp metal procedure must be maintained.
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3.7 Metal Detector procedure must be followed.
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3.8 Dedicated qualified Metal Detector Operator are available
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3.9 Metal Detection Calibration report are availble.
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3.10 Metal Operator are Trained.
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3.11 Metal free zone is free for Matel
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3.12 1 Hour keeping area is available
4. Mold Control
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4.1 Mold Control policy & procedure
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4.2 Record of Humidity & temperature
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4.3 Communicate all about mold control procedure.
5. Pest Control
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5.1 Pest control policy & Procedure
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5.2 Record of pest control system.
6. Chemical Control
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6.1 Hazardous chemical list
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6.2 Chemical control policy and procedure must be followed.
Internal Audit
1. Audit
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1.1 Internal Audit Policy & Procedure
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1.2 Internal Audit plan, notice, checklist & Report
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1.3 Internal Auditor Qualification & Job Description.
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1.4 Corrective & Preventive Action plan
Improvement
1. Evaluation & Monitoring, Performance & Feedback
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1.1 Supplier Evaluation, Selection, Monitoring Procedure.
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1.2 Supplier Performance data
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1.3 Customer Feed back data
2. Traceability
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2.1 Record of entire Product traceability system
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2.2 Verification of Product traceability
Pictorial Evidence
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A. Factory/Organization Information
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B. Quality Management System
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C. Planning and Management Review
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D. Resources
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E. Sample Requirements
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F. Manufacturing
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G. Product Safety & Integrity
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H. Internal Audit
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I. Improvement