Can a non AS9100 facility build a Aerospace product?

Q

quality1

#1
#1
Hi All,

Can a non AS9100 facility of your company build an aerospace product (cables) and the 9102 be performed at another facility who's AS9100? Customer did not specified where cables are to be built?

Thank you for your help
 
GAGEpack - Gage & Calibration Management
Elsmar Forum Sponsor
R

Reg Morrison

#2
#2
AS9100 has requirements for work transfer and outsourcing processes. If the customer was led to believe that the product was being built in one specific location, what you are asking goes against AS9100 and ethical practices.

If the customer knew that the harnesses would be built elsewhere, then the question would have been unnecessary, isn't it?
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
Q AS9100 Repairs - Approval from a non-aerospace customer prior to conducting a repair AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 14
K AS9100 Certification of a Non-Aerospace Company AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
C AS9100 8.3 Procedure for Non-Conforming Parts - When should an NCR be filled out? Nonconformance and Corrective Action 5
M AS9100 First Article - Does 7.5.1.1 revC or 8.2.4.2 revB apply to Non Aerospace Goods AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 19
B Traveler and Router Systems - AS9100 Aerospace Products vs. Non-Aerospace Products AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 17
J AS9100 Control of Non Conforming Product - Personnel who make Disposition Decisions AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 31
B How maintain an AS9100 QMS that allows us to produce non-AS product AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
O AS9100 for 'Non Production Part' Company - We make check fixtures AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 13
A Applicability of AS9100 Standards to Non Aerospace Products AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
S First Article Inspection in an AS9100 service industry (Final product non tangable) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 13
Q API Spec Q1 9th Ed 4.4.2 Non-conformance Oil and Gas Industry Standards and Regulations 8
T Do I need to add non-product related service providers to my ASL? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 12
J ISO 13485- 8.3.1 Non-conforming material high volume ISO 13485:2016 - Medical Device Quality Management Systems 4
F MSA for non-contact CMM - ISO10360 Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 0
M Using a Non Certified vendor Supplier Quality Assurance and other Supplier Issues 5
somashekar Justification for Non-applicable clause at Stage 2, in clause 4. ISO 13485:2016 - Medical Device Quality Management Systems 11
Z Swiss Authorized representative & non-medical device regulations Other Medical Device Regulations World-Wide 0
R Lead auditor scenario (Need help) is this non conforming to ISO13485 Manufacturing and Related Processes 2
D Help Me. Non conformitty in External Audit IATF 16949 - Automotive Quality Systems Standard 13
S Electronic Signatures - Non-Conformance - ISO 13485:2016 ISO 13485:2016 - Medical Device Quality Management Systems 30
S Do you follow your QMS for non-device software features? Medical Information Technology, Medical Software and Health Informatics 4
J Can we register non-device clinical decision support software under draft guidance? Other US Medical Device Regulations 5
D IATF 16949 SI 10, External non-accredited lab IATF 16949 - Automotive Quality Systems Standard 4
M Selling non-CE marked devices for evaluation EU Medical Device Regulations 4
T Non API products need to comply to API Q1? Oil and Gas Industry Standards and Regulations 3
L "Shelf-Life" Class I Non-Sterile Products Expiration Date? CE Marking (Conformité Européene) / CB Scheme 3
B Process / Procedure - Radiographic (X-Ray) Non-Film Document Control Systems, Procedures, Forms and Templates 0
N How to find column number for the last non-empty column? Using Minitab Software 0
A Need to calculate tolerance Intervals with a set of non-normal data and 3-Parameter Weibull distribution Using Minitab Software 0
3 Non-conformance Register vs Corrective Action Register ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 13
G Competent Authority non-EU Manufacturer EU Medical Device Regulations 7
F Non conforming locked? Manufacturing and Related Processes 13
M Changing Investigational Device from Non-Sterile to Sterile - what are the implications? Other Medical Device and Orthopedic Related Topics 3
K Is Calibration Required for Non-Adjustable Commercial Inspection Devices? General Measurement Device and Calibration Topics 11
J Informal vs formal scope creep... managing non-medical devices through system processes ISO 13485:2016 - Medical Device Quality Management Systems 2
G Not accepting a non conformity during an audit General Auditing Discussions 11
J In-house (NHS) manufacture and use (by staff) of non-medical devices.. any regulations apply? UK Medical Device Regulations 6
B Does FDA Registration QSR need to cover non-medical devices for contract repackager? US Food and Drug Administration (FDA) 1
A Brexit Mandate for EU Authorised Representative for non medical devices CE Marking (Conformité Européene) / CB Scheme 7
E Accredited vs. non-accredited labs for 60601 compliance in the US IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
E Accredited vs. non-accredited labs for 60601 compliance in the US Other Medical Device Related Standards 4
C Non-sterile reusable surgical instruments - FDA sterilization requirement Other Medical Device Related Standards 2
L Water requirement for Non-sterile topical OTCs Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 0
B Procedure packs with non-medical devices EU Medical Device Regulations 1
W Non Sterile Medical Device Environmental Tests Other Medical Device Related Standards 4
S Advice on how to reduce overhead of handling non-conforming material Nonconformance and Corrective Action 7
G Team to analyze a non conformance Customer Complaints 26
J Promoting and marketing of a non approved device 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 6
G 0 non conformities in registrar audits over 4 years Management Review Meetings and related Processes 12
K CE Marking Class 1 (Non sterile) medical device CE Marking (Conformité Européene) / CB Scheme 3

Similar threads

Top Bottom