Part Approval - Eliminating Incoming Quality Inspection by Customer

J

Johnny Chow

#1
Part Approval and IQC

From: "Johnny Chow(QA-M200)"
Subject: PART APPROVAL & IQC
Date: Mon, 7 May 2001 11:32:20 +0800

Dear Forum,

I hope to seek yr professional advice on the below.

We have a Business Unit doing Contract Manufacturing or OEM. And the unit is currently buying and assemble parts - machine parts, electrical and mechanical std parts prior finished goods delivery.

Our customer insist that no incoming inspection and no Part Approval at the initial start and incoming material. He put it that the vendor must supply according to the spec given. The vendor selection and approval process must ensure that we got the right supplier. Emphasis on purchasing control too.

But I thought the other way round. No inspection. How to establish ? What criteria and judgement presented ? Or I further stressed at least a Part Approval process must be run to review the vendor process capability and the ultimatum the part's quality of fulfilling the dwg. But he indicated that vendor's process shall be done during vendor qualifcation.

We're seeking this BU for ISO 9000 scope extension audit very soon ?

Pls advise.

BR
Johnny Chow
Corporate QA Manager
Scarborough (HK) Ltd
Tel : (86)-769-2172178 Ext : 662
Fax : (86)-769-2171193
 
Elsmar Forum Sponsor
D

D.Scott

#2
Johnny - sounds like your customer is telling you HE doesn't want to do incoming inspection and expects you to ensure your supplier meets the requirements. I don't see this as telling you that you can't use incoming inspection or whatever else(including PPAP) to qualify your supplier. It would make sense that you use whatever practice you feel gives you confidence that you are purchasing good product, then maintain your own controls to ensure your customer is satisfied.

If this situation came up with one of our customers, I would go through the entire PPAP process and hold the information internally. This way I would feel confident that my process was meeting the requirements too.

Do what you always do to ensure conformance to customer requirements and you shouldn't go too far wrong. Trying to re-invent the wheel could lead to confusion and errors.

Dave
 

Howard Atkins

Forum Administrator
Leader
Admin
#3
I have difficulty in properly understanding.
You are assemblying parts and your customer does not want to check them.
You though must know wether the parts you receive are good and if your process is also correct.
I agree with Dave, request and approve PPAP from your supplier and produce and internal PPAP for yourselves.
I understand why you customer does not want to inspect but I do not understand why he does not want to approve an initial part.
Without this approval how can there be an agreement on an aceptable part!!!
Good Luck
 

Marc

Fully vaccinated are you?
Leader
#4
From: "Johnny Chow(QA-M200)"
Subject: APQP & IQC
Date: Tue, 8 May 2001 08:48:04 +0800

Dear Forum member,

Thank you for initiating this forum.

I wish to add to my points. This customer is a UK company. We're his localization manufacturer here in China. The customer Mr R is from the parent company, UK Procurement Manager. And now he's also responsible to run the BU as the Div Manager.

He insisted no incoming inspection because he thought his parent company could be doing so. He also advised me to visit his company to see for myself. He's also selling the idea of TQM, no inspection and everybody will just be responsible for his job. Quality should be built-in. This customer I mean Mr R will be happy if I just follow him. I found that he preaches a lot of TQM stuff but hardly understand how to make it best to application. Well he's not a Quality guy anyway.

I wish to stand firm on this. Customer is not always right. I felt he does not understand the ISO 9000. I'm questioning what element of ISO 9000 1994 version or 2000 version will be best suited to hit this precisely. I know QS 9000 would easily solve this issue.

Thanks for your professinal advice. This forum is great.

I find no way to go in via the forum web. Therefore I put in thru Contact Us. Could you lead me correctly.

BR
Johnny Chow
Corporate QA Manager
Scarborough (HK) Ltd
Tel : (86)-769-2172178 Ext : 662
Fax : (86)-769-2171193
 
S
#5
Johnny, You state,
"We have a Business Unit doing Contract Manufacturing or OEM. And the unit is currently buying and assemble parts - machine parts, electrical and mechanical std parts prior finished goods delivery."

I wiil assume that you have work instructions and in-process inspection.

"1- Our customer insist that no incoming inspection and no Part Approval at the initial start and incoming material. 2-He put it that the vendor must supply according to the spec given. 3-The vendor selection and approval process must ensure that we got the right supplier. 4-Emphasis on purchasing control too."

1- This is acceptable, but requires a lot of contact with the customer.
2- Correct
3- Correct, if you are selecting the supplier, then you need to make sure he can do the job.
4- Excellent idea. QC should work in concert with purchasing.

"1-But I thought the other way round. No inspection. How to establish ? What criteria and judgement presented ? 2-Or I further stressed at least a Part Approval process must be run to review the vendor process capability and the ultimatum the part's quality of fulfilling the dwg. 3-But he indicated that vendor's process shall be done during vendor qualifcation"

1- You are correct in your thinking. I would suggest that you do some receiving inspection to establish the comfort zone with your supplier.

2- Again you are correct, a part approval should be required.

3- I agree. What your customer wants is similar to the "Daimler/Chrysler" Process Sign Off (PSO). This is a team made up of representatives from the supplier and customer (You) that meet at the suppliers facility and approve/disapprove the product and the process.

Your customers request is not off base. There are a lot of companies that work this way, including automotive suppliers. In fact the "Big 3" does the same thing.

IMO the concept will work if you establish a good working relationship with your supplier.

In you following post you state;
" 1- I wish to stand firm on this. Customer is not always right. 2- I felt he does not understand the ISO-9000. 3- I'm questioning what element of ISO-9000 version will be best suited to hit this precisely"

1- True, but he pays the bills.

2- Neither does anyone else. We all interpret it differently. We just have to arrive at a consensus of understanding.

3- 4.10.2.1, Key word "otherwise verified".

Strictly my opinions. I hope I haven't confused the issue too much.
 
Thread starter Similar threads Forum Replies Date
Sidney Vianna AS9100 News PPAP in the Aerospace Sector - What is it? AS9145 - Requirements for Advanced Product Quality Planning and Production Part Approval Process AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
H Informational What is PPAP (Production Part Approval Process)? APQP and PPAP 26
S If a piece of software receives approval as part of a medical device system Canada Medical Device Regulations 5
J Differences between a Risk Management Plan vs. Production Part Approval Process AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
M Can an organisation hold an EASA Part 145 approval WITHOUT a QMS EASA and JAA Aviation Standards and Requirements 1
K FAI (First Article Inspection) vs PPAP (Production Part Approval Process) APQP and PPAP 16
A EASA Part 21G approval for manufacturing of seat covers, carpets, curtains & others EASA and JAA Aviation Standards and Requirements 1
P Tier 2 Part Approval where Painting is Outsourced APQP and PPAP 2
J PPAP (Production Part Approval Process) Requirements for Annual Revalidations APQP and PPAP 1
somashekar Document Approval per Sec. 820.40 (a) of 21 CFR part 820 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
L Do I need to use an EASA Part 21 approval, to upload software on a Transport Category EASA and JAA Aviation Standards and Requirements 2
M PPAP (Production Part Approval Process) files for Ford APQP and PPAP 11
M Part & Process Approval in Medical Devices Other Medical Device and Orthopedic Related Topics 3
A What is PPAP (Production Part Approval Process) Why submit it and/with PSW APQP and PPAP 2
P PPAP Approval - Customer approval of PSW (part submission warrant) APQP and PPAP 5
B Help for beginner - PPAP (Production Part Approval Process) APQP and PPAP 9
F EASA Part 21 Subpart J - Understanding the DOA (Design Organization Approval) EASA and JAA Aviation Standards and Requirements 23
R Is Kappa Study Required during PPAP (Production Part Approval Process)? IATF 16949 - Automotive Quality Systems Standard 9
T Production Part Approval Process (PPAP) Presentation in ppt. format APQP and PPAP 3
F Who should Sign Supplier PPAP (Production Part Approval Process) documents? APQP and PPAP 13
H Who can require PPAP (Production Part Approval Process)? APQP and PPAP 7
S Tell Me All About PPAP (Production Part Approval Process) APQP and PPAP 7
D Source Control Drawing vs. Part Approval Process Document Control Systems, Procedures, Forms and Templates 9
J Are email acceptable as records? Email for a customer approval of some part? Records and Data - Quality, Legal and Other Evidence 20
H First Part Approval - Large Construction Vehicles APQP and PPAP 3
T Customer Part Approval Process Manual? IATF 16949 - Automotive Quality Systems Standard 6
J AIAG PPAP (Production Part Approval Process) Manual Fourth Edition Released APQP and PPAP 69
A PPAP (Production Part Approval Process) - Where can I buy the AIAG Manual? Preventive Action and Continuous Improvement 2
J PPAP (Production Part Approval Process) Submission Level Differences - Forms attached APQP and PPAP 17
S Students trying find information on Producation Part Approval Process - ABC of PPAP APQP and PPAP 2
W PPAP (Production Part Approval Process) - Clarify When submission is required APQP and PPAP 10
S GR & R studies for 16 Cavity part Manufacturing and Related Processes 12
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 9
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
M Part submission warrant with every rev up of drawings APQP and PPAP 2
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
I Restricting scope to one part number for one customer IATF 16949 - Automotive Quality Systems Standard 6

Similar threads

Top Bottom