PPAP documentation. ▪ After development is complete and before series delivery, the product is released in accordance with PPAP documentation as per VDA or AIAG. ▪ Requirements for PPAP creation: OEM/ project/ article/ customer reference number/ color/ design/ lamination/ IMDS ID of the requesting customer. ▪ The customer is provided with 2 DIN A4 samples for each PPAP documentation; additional samples can be purchased for an extra charge of €5/sample. ▪ In the event of subsequent changes to the PPAP documentation of the customer or the processing plant, the change will be charged at a flat rate of €250.
PPAP documentation. 8.1.1. PPAP (Production Part Approval Process) o PPAP is a series of documents for automotive industry. With them, the Supplier shall prove the characteristics of the Production Part and consistency (stability) of its processes. The Supplier shall undertake to present the documents (PPAP – minimum level 3) within the agreed period of time. o On the basis of a PPAP binder, the Customer shall release its regular production. PSW (Part submission warrant) is used as the release document. o In the event of an inconsistent process and Production Part's non- conformity being found, the Customer shall reserve the right to revoke the validity of PSW. o Subject to an agreement with the Customer, PPAP can be used also for non- automotive industry branches. o Subject to an agreement with the Customer, other documents than PSW, such as Release Report RR, EMPB etc., can be used for the release of production. o PPAP is further explained in the annex to this Agreement.
8.1.2. During individual phases of Production Part creation, the following quality assurance measures should be planned and adopted: - Verification of Production Part design D-FMEA; verification of process P- FMEA; o FMEA includes: Recognition of possible defects Correction of possible defects and consequences in the design and process o Each subsequent change in the Design and Process requires a modification of FMEA o The Supplier should submit the D-FMEA to the Customer for the approval and authorisation of the Design. - Planning of testing technology, testing devices, testing characteristics; - Analysis of machines capability; Cmk ≥2.00 and processes capability Cpk ≥1.67 (unless otherwise agreed); - Proofs of meeting the reception requirements; - Planning of system, processes and Production Parts assessments. - Samplings, performed in accordance with an order, i.e. performed by the Supplier after each change / correction; o Samplings are performed separately for individual Production Parts (e.g. in the case of plastic parts, each nest should be sampled etc.); o With a view to the valid documentation, all samplings should be documented in test reports and measurement protocols; o In the event of identified deviations, reports with corrective measures should be prepared; o For each sampling, the assessment of all quality and functional characteristics should be performed, as well as statistic assessment for characteristics in accordance with the Quality Documentation; o Tests and measurements results a...
PPAP documentation. Supplier will provide PPAP documentation according with customer drawings at a level 3, unless MLNA/MLMX require a different level of PPAP documentation. Supplier will cover all expenses of PPAP documentation.
