| One of the requirement of ISO TS 16949 standard is the PPAP - Production Part Approval Process (4th Edition): The purpose of PPAP is to provide the evidence that all customer design record and specification requirements are properly understood by the organization and that the manufacturing process has the potential to produce product consistently meeting these requirements during an actual production run at the quoted production rate. PPAP is applicable to an organization that supplies standard catalog production or service parts which complies with PPAP unless formally waived by the authorized Customer Representative. The organization must submit for PPAP approval prior to the first production shipment in the following situations unless the authorized Customer Representative has waived this requirement 1. New part or product (i.e. a specific part, material, or color not previously supplied to the customer), 2. Correction of a discrepancy on a previously submitted part, 3. Engineering change to design records, specifications, or materials for production product/part number(s)
Process technology new to the organization, not previously used for this product.
PPAP requirements:(19 records of PPAP) 1.Design Records 2.Customer Engineering Changes Records 3. Customer Engineering Approval 4. Design FMEA (If the organization is product design-responsible) 5. Process Flow Diagram(s) 6. Process FMEA 7. Control Plan 8. MSA Studies 9. Dimensional Results 10. Records of Material / Performance Test Results 11. Initial Process Studies 12. Qualified Laboratory Documentation 13. Appearance Approval Report 14. Sample Production Parts 15. Master Sample 16. Checking Aids 17. Records of Compliance 18. Bulk Material Checklist 19. Part Submission Warrant (PSW) Contact for ISO TS 16949 Certificate, ISO TS 16949 Consultancy, ISO TS 16949 Certification, ISO TS 16949 Audit, ISO TS 1949 Training, ISO TS 16949 Training to students.
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