Supplier Certificate Suspended in OASIS - Do we need stage 1 and 2 to reinstate cert?

B

Blankford

#1
#1
If a supplier goes into suspension due to lack of effectively closing prior NCR's, do they have to start over with a Stage 1 & Stage 2 only if it is a Recertification audit or does that also apply for surveillance audits?
 
Elsmar Forum Sponsor
Sidney Vianna

Sidney Vianna

Post Responsibly
Staff member
Admin
#2
#2
Re: Supplier Certificate Suspended in OASIS - do we need stage 1 and 2 to reinstate c

According to my recollection of the AS9104/1 Standard, you would not need a stage 1 & 2 re-audit to reinstate the validity of the certificate, UNLESS, due to the suspension, the certificate validity expired and the reinstatement could not be accomplished before the expiry date.
 
B

Big Jim

Super Moderator
#3
#3
Re: Supplier Certificate Suspended in OASIS - Do we need stage 1 and 2 to reinstate c

This is a question for your certification body.

If the certification is withdrawn, then, yes, you need to start over. If it is suspended, I'm not sure. Suspension is not the same as a withdrawal.
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
noratkhen Eligibility to get a IATF 16949 certificate for a Tier N>3 supplier? IATF 16949 - Automotive Quality Systems Standard 25
K Reviewing a supplier's ISO 9001 certificate issued for a future date Registrars and Notified Bodies 10
A Supplier's remote site is not on their ISO 9001 Certificate ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
R Supplier Certificate of Conformity/Conformance Standard Other ISO and International Standards and European Regulations 3
T COA (Certificate of Analysis) issued from supplier - His name or mine? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 16
R On/OFF switch received from supplier - No CE marking but with Certificate CE Marking (Conformité Européene) / CB Scheme 1
L Certificate of Conformity? Supplier incoming material inspection CE Marking (Conformité Européene) / CB Scheme 3
W Eligibility of Tier 2 supplier of forged parts to get TS 16949:2002 certificate IATF 16949 - Automotive Quality Systems Standard 13
L Supplier QMS certificate accredidation - Certificate has no logo ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 10
O Certificate of Compliance for a Vendor (Supplier) - Looking for an example Inspection, Prints (Drawings), Testing, Sampling and Related Topics 8
SteelMaiden Customer's Internal Audit - SQA - Supplier ISO 9001 Certificate Expired Internal Auditing 11
T PPAP requirements - Supplier's supplier's quality certificate and IMDS documentation RoHS, REACH, ELV, IMDS and Restricted Substances 31
S Supplier lost QS certificate and gave no notification Supplier Quality Assurance and other Supplier Issues 2
K Outsourcing Processes - Supplier CofC (Certificate of Conformance) Supplier Quality Assurance and other Supplier Issues 17
J Supplier not responding to PPAP request APQP and PPAP 5
D Supplier audit Medical Device and FDA Regulations and Standards News 2
lanley liao Does all of the suppliers need to integrated into the supplier list qualified of the company? Oil and Gas Industry Standards and Regulations 2
S Distinction between a critical supplier and a Virtual manufacturer EU Medical Device Regulations 2
R AS9102 FAI Change in Material / Process Supplier AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
John Broomfield Five ways to botch your supplier management program Misc. Quality Assurance and Business Systems Related Topics 7
C Supplier survey - 200 to 250 duppliers Supplier Quality Assurance and other Supplier Issues 3
J Where is the definition of a critical supplier? ISO 13485:2016 - Medical Device Quality Management Systems 5
U Approved Vendor (supplier) List Supplier Quality Assurance and other Supplier Issues 8
M Supplier requirements - Major supplier is a Non-Profit registered with ICCBBA (FDA UDI) Supply Chain Security Management Systems 12
P Training department ideas and development for automotive supplier Training - Internal, External, Online and Distance Learning 6
B Software service provider as critical supplier ISO 13485:2016 - Medical Device Quality Management Systems 5
T AS9100D Clause 10.2.1g Supplier Corrective Action for each and every nonconformity? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
S Supplier protocol for the Quality Supplier Quality Assurance and other Supplier Issues 6
A API Spec Q1 Purchasing Process - Supplier Reevaluation based on Supplier Risks 5.6.1.4 Oil and Gas Industry Standards and Regulations 17
D Approved supplier list - Distributors question ISO 13485:2016 - Medical Device Quality Management Systems 6
G Supplier delivered recent PPAP, should he deliver yearly layout inspection? IATF 16949 - Automotive Quality Systems Standard 4
E ISO 13485 QMS certification as a Supplier ISO 13485:2016 - Medical Device Quality Management Systems 8
G Supplier doesn't share drawings IATF 16949 - Automotive Quality Systems Standard 15
S Use of raw materials by two supplier CE Marking (Conformité Européene) / CB Scheme 2
D Are Supplier Quality Agreements Quality Records ? Other Medical Device Regulations World-Wide 9
G Dealing with non conformity caused by Supplier Components detected in the production line IATF 16949 - Automotive Quality Systems Standard 14
G Supplier doesn't accept the complaints Supplier Quality Assurance and other Supplier Issues 20
K New supplier audit as per V3.1 by French Automotive OEM General Auditing Discussions 2
A ASL requirement when the supplier is certified for ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 6
S Supplier Management ISO 13485: 2016- Which supplier needs to fill in a self assessment form? ISO 13485:2016 - Medical Device Quality Management Systems 6
D Approved supplier list for R&D ISO 13485:2016 - Medical Device Quality Management Systems 5
M SemaTech SSQA Standardized Supplier Quality Assessment - my favorite tool ever Manufacturing and Related Processes 1
D Supplier Quality level category help - high level ISO 13485:2016 - Medical Device Quality Management Systems 6
J Supplier Controlled Shipping (GM CS1) Condition Manufacturing and Related Processes 3
L Supplier within the Organization ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
D Supplier Quality - How to classify a supplier level Medical Device and FDA Regulations and Standards News 10
P Understanding DFMEA and PFMEA - Supplier Related IATF 16949 - Automotive Quality Systems Standard 21
S Can assembly manufacturing sub-supplier be certified IATF 16949? IATF 16949 - Automotive Quality Systems Standard 6
M How Supplier Capacity check is done by competitors Manufacturing and Related Processes 0
C One Time Service Supplier - Temperature and Humidity Testing Service ISO 13485:2016 - Medical Device Quality Management Systems 5

Similar threads

Top Bottom