Part Submission Warrant - Omitting Parts of

M

Mike48

#1
:bigwave:

The company I work for made a slight modification to the PSW as found in the PPAP manual. They deleted the second line of the note that states "Are plastic parts identified with appropriate ISO marking codes." I advised against this because I thought all of this material was proprietary, and availabe only for our use as is. Any comments?
 
Elsmar Forum Sponsor
A

Al Dyer

#2
See AIAG PPAP Manual page 15 Note 2. While copies are allowed, I would think deletions from the form would be frowned upon.
 
D

D.Scott

#3
I agree Al

But if we are taking a vote, I would be in favor of deleting the "run at rate" section. :biglaugh:

Dave
 

Howard Atkins

Forum Administrator
Leader
Admin
#5
IMHO delete what you want. The question is whether your customer will accept it.
If he accepts it no problem, but if not.........
You will have to resubmit.
 
Thread starter Similar threads Forum Replies Date
M Part submission warrant with every rev up of drawings APQP and PPAP 2
J Part submission warrant for Level 1 PPAP APQP and PPAP 1
J PSW (Part Submission Warrant) and Design Requirements APQP and PPAP 14
S Looking for a PPAP PSW, Part Submission Warrant, in Chinese APQP and PPAP 5
Moncia Part Submission Warrant - Customer Requirements for PSW Submission APQP and PPAP 7
D PSW (Part Submission Warrant) Question for Part Number Change APQP and PPAP 9
V Safety and/or Government Regulation question on a PSW (Part Submission Warrant) APQP and PPAP 6
V Is it OK to put 2 Part Numbers on 1 PSW (Part Submission Warrant)? APQP and PPAP 12
V What has more weight: Master Print or Part Submission Warrant? APQP and PPAP 4
A Does the PSW (Part Submission Warrant) need to be a controlled document? APQP and PPAP 7
automoto PPAP Forms - Part Submission (Warrant) form .xls Document Control Systems, Procedures, Forms and Templates 2
E PSW (Part Submission Warrant) for Service Parts APQP and PPAP 4
P PPAP Approval - Customer approval of PSW (part submission warrant) APQP and PPAP 5
S Material Supplier Part Submission Warrant (PSW) APQP and PPAP 2
I Confused on PPAP re-submission - Help on PSW (Part Submission Warrant) APQP and PPAP 3
M Spanish PSW (Part Submission Warrant) Needed APQP and PPAP 8
W Better Understanding of PSW (Part Submission Warrant) APQP and PPAP 7
B New PSW (Part Submission Warrant) - 4th Edition PPAP Manual APQP and PPAP 38
G Part Submission Warrant (PSW) dispute APQP and PPAP 19
S Can anybody tell me what the legal status of the Part Submission warrant (PSW) is? APQP and PPAP 4
D Seeking CURRENT PPAP Part Submission Warrant APQP and PPAP 7
D Truck Industry Part Submission Warrant APQP and PPAP 6
G Gage R&R - Where am I going wrong? Part of a FAIR submission (Aerospace) Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 2
JoCam Approving a Test House on a Medical Device as a part of a 510k Submission 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
S Is a Quality Manual part of a 510k Submission? Other US Medical Device Regulations 1
C Who in the supplier organization has to sign the PSW (Part Submission Warranty)? APQP and PPAP 6
P Part Submission Form - Need to submit PSW only once? APQP and PPAP 5
T Who signs PSW's? (PPAP Part Submission Warrants) APQP and PPAP 1
shimonv Bench Testing as part of 510(k) Submission US Food and Drug Administration (FDA) 1
B Salary Requirements as part of initial resume/CV submission Career and Occupation Discussions 13
B Quality Stand Down form - Part of a PPAP submission to Johnson Controls Document Control Systems, Procedures, Forms and Templates 12
C New PPAP submission required when changing part number? APQP and PPAP 11
J PPAP (Production Part Approval Process) Submission Level Differences - Forms attached APQP and PPAP 17
W PPAP (Production Part Approval Process) - Clarify When submission is required APQP and PPAP 10
A Has anyone implemented the Adobe Acrobat Sign Validation Pack to be 21 CFR Part 11 Compliant? ISO 13485:2016 - Medical Device Quality Management Systems 1
H Looking to make inspection faster for part with over 100 dimensions. Inspection, Prints (Drawings), Testing, Sampling and Related Topics 5
S FCC Part 15, 18 harmonized to a standard? Various Other Specifications, Standards, and related Requirements 3
PQ Systems SQCpack Tech Tuesday Webinar 4-Part Series Using SQCpack Software 0
K Device part of combination product certification requirements Medical Device and FDA Regulations and Standards News 3
L "to be treated as APPLIED PART": is shopping in requirements allowed? IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
X Separation of battery powered FB type applied part IEC 60601 - Medical Electrical Equipment Safety Standards Series 3
N Direct Part Marking of the "CE" symbol- Class I Device EU Medical Device Regulations 1
P Controls over Systems Documentation in 21 CFR Part 11 Qualification and Validation (including 21 CFR Part 11) 1
R Separation and PE Requirements of a Type B Applied Part IEC 60601 - Medical Electrical Equipment Safety Standards Series 3
P Part 21G - Liabilities of a Quality Manager Form 4 Post Holder EASA and JAA Aviation Standards and Requirements 4
W Part 145 Maintenance Data Review EASA and JAA Aviation Standards and Requirements 1
C Part selection for Faro arm MSA Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 7
R Understanding ISO12944 (Part 4) Manufacturing and Related Processes 6
E Performing a GRR when you get multiple readings over time per part. Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 5
K 13485 do e-signatures have to be 21 CFR Part 11 compliant? ISO 13485:2016 - Medical Device Quality Management Systems 8

Similar threads

Top Bottom