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Design Record
π SAMPLE PRODUCT AND RETENTION OF PPAP MASTER SAMPLES
Unless otherwise specified by MPT, has supplier submitted 6 parts used for dimensional verification? These shall be labeled with part#, cavity, revision, tool#, etc. & with a sample number that corresponds to the dimensional report.
Has supplier submitted samples that clearly identify each unique cavity, mold, line, etc.?
Are the sample parts taken from a significant production run as outlined in the AIAG PPAP Manual?
Has supplier retained master samples at supplier end with unique identification for part#, cavity, revision, tool#, etc. & with a sample number that corresponds to the dimensional report?
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