QSB+ revoked - Notify registrar, what's next?

soulmas

Involved In Discussions
#1
Hi!

If QSB+ is revoked and GM is requesting the organization to notify the registrar, what the registrar will do?
On the IAOB clarification of the impact of customer special, it does not define if the QSB is revoked, the registrar will open a major or minor NC to the organization.. does anyone knows what the registrar will do?

thank you,
Soulmas
 
Elsmar Forum Sponsor

John Broomfield

Staff member
Super Moderator
#2
Soulmas,

It will determine the effectiveness of your corrective action (removal of root causes to stop recurrence) to establish or re-establish your Quality System Basics to satisfy GM's requirements.

John
 

soulmas

Involved In Discussions
#3
Thank you John... that's what I thought.. however, the question is, is it going to be a major or a minor NC with the registrar? do you know?
 

John Broomfield

Staff member
Super Moderator
#4
Soulmas,

If your management system is missing an entire component or process then you are probably looking at a major.

...but no matter you should already be well into your corrective action before the registrar visits.

John
 
Thread starter Similar threads Forum Replies Date
M QSB plus given by PSA and GM and ISO TS 16949 IATF 16949 - Automotive Quality Systems Standard 2
K Fast Response Tracking Board (QSB+) Customer and Company Specific Requirements 6
A What is QSB? How do you implement? What are your documents? IATF 16949 - Automotive Quality Systems Standard 4
A Pls provide some examples of Quality System Basics (QSB) Internal Auditing 3
V QSB Layered Process Audits GM/OPEL Customer and Company Specific Requirements 3
M What do 'Read Across', 'Drill Deep' & '6 Panels' mean in GM's QSB Sheet? IATF 16949 - Automotive Quality Systems Standard 2
R GM (General Motors) QSB Fast Response Program Customer and Company Specific Requirements 12
N Contamination Control required by GM in QSB Implementation Document Control Systems, Procedures, Forms and Templates 5
B GM's QSB - Requirement, Checklists needed - Checklist used by GM to assess & sample Customer and Company Specific Requirements 9
B General Motors QSB (Quality System Basics) - Standard work instructions IATF 16949 - Automotive Quality Systems Standard 3
M GM's QSB (Quality System Basics) - Checklist for Control Plan Audit development. FMEA and Control Plans 4
L What is QSB Training? It's a GM thing - 'Quality System Basic' Training Training - Internal, External, Online and Distance Learning 19
J What are the actual requirements for QSB? IATF 16949 - Automotive Quality Systems Standard 21
Roberticus Reinstatement of Revoked Certification for NDT per NAS 410 8.4 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
A Q1 Revoked. How does this affect TS 16949? IATF 16949 - Automotive Quality Systems Standard 5
Sidney Vianna News you don't see everyday - Certification revoked Registrars and Notified Bodies 0
L Manufacturing site expansion - When to notify your NB EU Medical Device Regulations 3
B IATF certificate suspended - Who do we notify? IATF 16949 - Automotive Quality Systems Standard 6
L Reasons to submit a new PPAP or notify the customer APQP and PPAP 3
P Notify Registrar of Escalation letter IATF 16949 - Automotive Quality Systems Standard 1
C What are rules to notify customers if IATF cert is put on hold? IATF 16949 - Automotive Quality Systems Standard 2
E Manufacturer's responsibility to notify the NB regarding Medical Device End-of-Life CE Marking (Conformité Européene) / CB Scheme 1
R Is it a requirement to notify my customer if I receive a 483 from the FDA? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 6
M Class I Medical Device - Need to notify CA (Competent Authority) if selling in Asia EU Medical Device Regulations 4
K 510 (k) - Requirement to notify the FDA or is only the Notified Bodies required? Registrars and Notified Bodies 1
S Audit Notification - Is it a obligation to notify people or just good practice Internal Auditing 18
T How to Report/Notify Medical Device Software Changes to the FDA? US Food and Drug Administration (FDA) 3
E Do I need to notify the FDA of Management Representative changes? Other US Medical Device Regulations 3
S How to notify FDA of change of ownership? US Food and Drug Administration (FDA) 16
V When to Notify Customer about Die Modification APQP and PPAP 4
M Minor/ Major Change - Japan - When you have to notify the PMDA of a change? Other Medical Device Regulations World-Wide 1
I EU Meddevs: Need to notify a new manufacturer to Notified Body? EU Medical Device Regulations 3
Z How to notify PMDA (Japan) on change of Legal Manufacturer? Japan Medical Device Regulations 6
B Process Change Notification (PCN) form to notify our customers of a change Document Control Systems, Procedures, Forms and Templates 3
R EU Medical Device Change Decision Tree (when to notify the NB) EU Medical Device Regulations 4
V Procedure to notify Health Canada, FDA and Japan Pal for Minor Design Changes Canada Medical Device Regulations 5
E Tips on how to notify customers (and potential ones) of ISO Certification ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
I Should We Notify Our Registrar - Has Our Scope Changed? IATF 16949 - Automotive Quality Systems Standard 5
M Material shelf of life expired - Notify Customer/Violate which clause? IATF 16949 - Automotive Quality Systems Standard 5
U-DOG Is there a need to notify your customers if your ISO 9001 certificate expires? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
J Chrysler Customer Specific Requirements - When to notify the registrar IATF 16949 - Automotive Quality Systems Standard 3
A Rework and PPAP - When should we notify the customer? QS-9000 - American Automotive Manufacturers Standard 2
S Supplier shall notify GM - II.3.3 Customer Notification of Supplier Initiated Changes APQP and PPAP 8
C Process Management - Consistent variability over time - Notify management? Misc. Quality Assurance and Business Systems Related Topics 11
G 4.1.6.1 Notify certif. body QS-9000 - American Automotive Manufacturers Standard 2

Similar threads

Top Bottom