In today's fast-paced manufacturing environment, adhering to strict quality standards is essential for success, which is where the AIAG PPAP Manual 4th Edition comes into play, particularly for industries like Cooper Industries. This comprehensive guide outlines specific requirements for the Production Part Approval Process (PPAP), providing a structured approach for suppliers to demonstrate their compliance with design records, engineering changes, and quality standards. The manual delineates five distinct PPAP submission levels, each catering to various parts and scenarios, ranging from "non-critical" parts to those requiring a complete review at the manufacturing location. Key elements include design records, FMEAs, control plans, dimensional results, and material testing, extending to specialized requirements like appearance approval and customer-specific necessities. With a focus on precision and adherence to detailed requirements, the manual serves as an indispensable desk reference for Cooper Industries' suppliers, guiding them through the submission process to ensure that all components meet stringent quality and reliability standards before entering production. The PPAP Manual underlines the importance of collaboration between suppliers and manufacturers, emphasizing the need for clear communication and thorough documentation to achieve product excellence and customer satisfaction.
Question | Answer |
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Form Name | Aiag Ppap Manual 4Th Edition Form |
Form Length | 1 pages |
Fillable? | No |
Fillable fields | 0 |
Avg. time to fill out | 15 sec |
Other names | aiag fmea 5th edition pdf download, aiag manual pdf, fmea manual 5th edition pdf download, fmea 5th edition pdf download |
PPAP |
Submission Requirements |
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Quick Reference |
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Production Part Approval Process |
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(For internal Cooper use Only!) |
Note: This document is meant as a desk reference for Cooper Industries PPAP submissions. Complete guidelines and definition are provided in the Cooper Industries PPAP manual. Application and defined requirements are at the discretion of your Cooper Divisionall Quality Representative. Contact them with any additional questions.
Element Order |
PPAP Requirements |
Level1 |
Level2 |
Level3 |
Level4 |
Level5 |
Required Documents |
Additional Comments and Clarity |
documents in this order. |
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AIAG PPAP Fourth Edition |
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Important: Submit your |
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1 |
Part Submission |
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AR |
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Cooper PSW only |
Cooper PSW is required for all submissions and required on all Cooper designed parts. |
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Warrant (PSW) |
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2 |
Design Records & |
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Cooper Divisional Part |
Include one clean copy of the current approved revision print with all dimensions, applicable specifications, and notes, |
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Bubbled part print(s). |
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bubbled (circle with corresponding number) on the print for reference to dimensional report. |
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3 |
Approved Engineering |
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Various engineering |
Any formal documentation that is not reflected in the current released print such as |
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Change Documentation |
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documentation |
engineering changes and any pertinent engineering correspondence. |
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4 |
Customer Engineering |
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Not Required for Cooper |
Not used with Cooper Industries submissions. |
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Approvals |
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Submissions |
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Can be Cooper FMEA |
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5 |
Design FMEA, |
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Format or an AIAG |
Required only if supplier is responsible for part design. |
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compliant DFMEA. |
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Any standard flowchart |
Identifies all process steps from receiving to shipping/warehouse operations. Must include all offline and in process |
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6 |
Process Flow Diagrams |
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inspections and testing including ongoing routine conformance checks such as annual dimensional layouts. Process steps |
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format. |
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must match PFMEA and Control Plan steps. |
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Can be Cooper PFMEA |
FMEA must be AIAG or comparable format that contains the same information as the AIAG form. Process steps must match |
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Process Flow Chart, Control Plan and address all characteristics associated with each operation. RPN numbers must be in |
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7 |
Process FMEA |
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Format or an AIAG |
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accordance with AIAG guidelines with critical processes and inspections identified. Recommended Actions for high RPN |
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compliant PFMEA. |
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totals are required. |
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Control Plan must be AIAG or comparable format that contains the same information. Must match the Flow Chart/FMEA |
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Can be Cooper supplied |
process steps and describe the actions of each phase of the manufacturing process from receiving to shipping/warehouse. |
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8 |
Control Plan |
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format or AIAG compliant |
All CTQs and SPC items must be addressed within the corresponding process step. Any dedicated check/testing fixtures |
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format. |
that are used will be identified along with the numbered characteristics it measures/verifies/tests on the print. All CTQ's |
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must be identified in the control plan. |
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Measurement System |
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Cooper GRR format or any |
Require an analysis of the capability of all measuring tools identified in the Control Plan (in process or offline) used in the |
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statistical package format |
decision making process of normal production. As a minimum gauge R&Rs, using percent of total tolerance must be included |
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Analysis Studies |
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for gage R&R. |
for all process tools used in determining acceptability of equipment measurement capability. |
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10 |
Dimensional Results |
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Must be on Cooper |
Cooper Dimensional Data Sheet is only acceptable format. |
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Dimensional report format |
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Certificates of Analysis for all primary raw materials such as chemicals, plastic resins and rubber. Chemical composition lab |
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Industry Standard reports |
reports for all metals and controlled substances. Performance life testing results such as salt spray, impact testing, heat, |
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Material, Performance |
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humidity, electrical performance, etc, when required either by print, specification or specific request by Cooper representative |
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or test result formats |
to be submitted on AIAG forms |
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Test Results |
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designated by Cooper |
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substituted with prior approval. AEC Qualification testing or equivalent is required for semiconductor devices. Any gaps |
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Industries. |
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between supplier qualification testing and AEC qualification testing requirements should be documented and approved by |
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Cooper Prior to submission. |
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Process Capability Study |
A short term study of process control capability (Cpk), must come from one continuous significant production run. At least |
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Initial Process Study |
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100 individual samples must be used for Cpk calculations. |
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using any statistical |
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(Cpk) |
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Supplier must have minimum Cpk value of 1.33 on all CTQs. No attribute data will be accepted for any PPAP submissions |
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package or Cooper |
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Capability Studies |
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for Initial Process Study. If CTQs are NOT identified on the print, the supplier will identify a minimum of two characteristics |
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Capability Data Forms. |
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that have a direct affect on fit, form, or function and perform Initial Process Studies on them. |
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A Quality Record that contains the specific tests/evaluations/calibrations that your facility performs, a list of your personnel's |
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13 |
Qualified Laboratory |
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Lab Scope and outside lab |
competency to perform these tests/evaluations/calibrations, a list of all measuring equipment used during production, and a |
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Documentation |
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proof of accreditation. |
list of methods and standards used to calibrate those tools. NOTE: All outside calibration or testing labs are required to |
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show proof of certification. |
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Appearance Approval |
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Needed only if part has color, grain, or some other cosmetic appearance requirement specified on the part print, or if |
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14 |
AR AR |
AR |
AR |
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AIAG format AAR |
specifically requested by Cooper to clarify a cosmetic requirement not clearly identified on a print. Format is AIAG form CFG- |
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Report |
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1002. |
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Parts tagged in |
The organization shall provide 3 sample parts WITH EVERY submission unless otherwise requested. |
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15 |
Sample Product Parts |
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accordance with Cooper |
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require 1 part per cavity. |
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PPAP reference manual |
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16 |
Master Samples |
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Required only for level 5 |
Not required for submission but must be maintained by the supplier. |
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Checking aids |
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Checking aid design prints |
Any part specific fixture, gauge, model or template. Tooling/gauges/fixtures must include design prints and a 3rd party layout |
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17 |
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and GRR for checking |
confirming conformity to print. |
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fixtures. |
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18 |
Customer Specific |
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Documents as specified by |
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Requirements |
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Cooper Industries |
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a |
Tooling Information |
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Specific Cooper Document |
Applies to all Cooper owned tooling. Typical application includes information and pictures on production tools such size, |
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Form |
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maximum cycles, ownership etc… |
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b |
Packaging Form |
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Specific Cooper Document |
Used to outline and verify both external and internal packaging requirements including any related testing. |
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c |
Inspection Plan |
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Specific ASC Format |
Specific format used by many ASC suppliers to document quality inspections |
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(ASC Suppliers only) |
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Specification Deviation |
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Used for any requirement that is |
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Specific Cooper Document |
submission. The supplier must provide a recommended action plan for any issue identified on the Specification Deviation |
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Form. |
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e |
Supplier PPAP |
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Specific Cooper Document |
To be submitted with every submission level except level 1 and must be signed by supplier representative. Used as both a |
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Checklist |
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reference/checklist tool as well as a verification that the right documentation is provided at the time of submission. |
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Cooper Industries PPAP Submission Levels (In compliance with AIAG Fourth Edition PPAP March 2006 release) |
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Level 1 |
Warrant only and Appearance Approval Report as requested submitted to the customer. Applied to: |
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applications and |
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Level 2 |
Warrant with product samples and limited supporting data submitted to the customer. Applied to: Critical Bulk products such as Plastic/PaintChemicals, critical fasteners, simple material |
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changes, simple revision level only changes or simple print updates not affecting |
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Level 3 |
Warrant with product samples and complete supporting data submitted to customer. Default Cooper Industries Submission Level Applied to: All new parts on Cooper programs. All changes |
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affecting |
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Level 4 |
Warrant and other requirements as defined by the customer. This level is reserved for special applications only. Applied to: This level can only be applied with prior approval from the designated |
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divisional Cooper Quality PPAP representative. |
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Level 5 |
Warrant with product samples and complete supporting data reviewed at the supplier's manufacturing location. Applied to: On site review as requested by each Cooper Division |
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Required for PPAP submission
Not required
Documents on a case by case basis are marked AR for "As Requested"
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IF Applicable |
IA |