The purpose of any Production Part Approval Process(PPAP) is to
confirm that the Supplier has properly understood all the design and
specification requirements for the components they supply and that the
supplier’s process has the capability to consistently deliver products that
comply with those requirements.
The PPAP approval often result in
a series of documents called PPAP Package used as a formal approval by the
supplier and customer. This package can contain Inspection Report.
The PPAP standard was initially
developed for the automotive industry. PPAP is now also used and adopted by
companies in many industries.
There are a lot of different
items that can make up a PPAP. Depending on the levels – from 1 to 5 – specific
documents might be required.
• Design Record(s) - A copy of
the drawing(s) that define the part to be supplied.
• Engineering Change Documents -
Documents that describe the change.
• Customer Engineering Approval -
Is used to demonstrate pre-approval by customers of a design.
• Design Failure Mode and Effects
Analysis, DFMEA - Shows evidence that all known potential failure modes of the
part design have been considered and addressed.
• Process Flow Diagram - Is used
to document all of the steps required to manufacture a part.
• Process Failure Mode and
Effects Analysis, PFMEA - Is used to show evidence that all known potential
failure modes of the manufacturing process have been considered and addressed.
• Control Plan - Defines how the
"potential failures" are inspected.
• Measurement System Analysis
(MSA) - Is used to determine and minimize the amount of total process
variability is due to variation in the measurement system.
• Dimensional Results - Is used
to document the measured values of all the inspection characteristics for the
design. The inspection characteristic numbers from the dimensional results
report should match the balloon numbers from the ballooned drawing.
• Material and Performance Test
Results - Is used to document all of the test results that aren't included in
the dimensional results. Additionally, this section lists all material
certifications as specified on the print. The material certification shows
compliance to the specific call on the print.
• Initial Process Study - Is used
to determine if the production process is likely to produce parts that meet
specification at the runs quoted.
• Qualified Laboratory
Documentation - A copy of the laboratory certifications (e.g. A2LA, etc...) of
the laboratories that performed the tests reported on the Dimensional Results
Report.
• Appearance Approval Report - Is
used to document customer approval of the physical appearance of the components
and usually refers to a specific appearance specification such as texture, colour,
etc...).
• Sample Parts - The parts used
to create the Dimensional Results and Material and Performance Test Results.
• Master Sample - A sample part
that is signed off on by the customer and supplier as a known good part. This
part is typically used to train inspectors on how to inspect subjective
characteristics.
• Checking Aids - Is used to
document and verify any special gages used to measure a part.
• Customer-Specific Requirements
- Refers to any special documents required by the customer that are not included
in the other PPAP items.
•
Part Submission Warrant, PSW - A summary of the entire PPAP package.
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