Common use of Production Part Approval Process Clause in Contracts

Production Part Approval Process. 7.12.1 The supplier shall demonstrate that the manufacturing processes have the potential to produce product consistently meeting these requirements. ▇▇▇▇▇▇ will identify the PPAP submission level based on the part criticality and function. -the- 7.12.2 ▇▇▇▇▇▇ Scientific requires PPAP submissions for approval of new or revised product. If required, the supplier shall not ship any production product until signed approval is received from ▇▇▇▇▇▇ Scientific per agreed method or documentation. 7.12.3 ▇▇▇▇▇▇ Scientific shall determine the PPAP level required. The ▇▇▇▇▇▇ Scientific PPAP owner shall work with the supplier to define the PPAP submission supporting data and the PPAP production run quantity. For product deemed critical to equipment function, a level 3 PPAP may be requested with a minimum; BOM verification, Dimensional Report, RoHS, and FMEA & Control Plan. 7.12.4 ▇▇▇▇▇▇ Scientific will provide a status of: Approved the product or service meets all requirements, and the supplier is authorized to deliver production quantities. Rejected the product or service fails to meet the requirements and the Supplier is not authorized to deliver the product or service. After implementing the corrective actions identified, the supplier must re- submit the PPAP to ▇▇▇▇▇▇ Scientific for approval. Interim Approval the product or service may be delivered for a specific time or quality while the supplier implements the required corrective actions. The supplier must re-submit the PPAP to ▇▇▇▇▇▇ Scientific for approval.

Production Part Approval Process. 7.12.1 The supplier shall demonstrate that the manufacturing processes have the potential to produce product consistently meeting these requirements. ▇▇▇▇▇▇ will identify the PPAP submission level based on the part criticality and function. -the-An example would be an “Off-the-shelf” item part with no critical features will only require a level one PPAP cover page submission. 7.12.2 ▇▇▇▇▇▇ Scientific requires PPAP submissions for approval of new or revised product. If required, the supplier shall not ship any production product until signed approval is received from ▇▇▇▇▇▇ Scientific per agreed method or documentation. 7.12.3 ▇▇▇▇▇▇ Scientific shall determine the PPAP level required. The ▇▇▇▇▇▇ Scientific PPAP owner shall work with the supplier to define the PPAP submission supporting data and the PPAP production run quantity. For product deemed critical to equipment function, a level 3 PPAP may be requested with a minimum; BOM verification, Dimensional Report, RoHS, and FMEA & Control Plan. 7.12.4 ▇▇▇▇▇▇ Scientific will provide a status of: ❖ Approved – the product or service meets all requirements, and the supplier is authorized to deliver production quantities. ❖ Rejected – the product or service fails to meet the requirements and the Supplier is not authorized to deliver the product or service. After implementing the corrective actions identified, the supplier must re- submit the PPAP to ▇▇▇▇▇▇ Scientific for approval. ❖ Interim Approval – the product or service may be delivered for a specific time or quality while the supplier implements the required corrective actions. The supplier must re-submit the PPAP to ▇▇▇▇▇▇ Scientific for approval.