Packaging and Damaged Parts returned from a Service Provider (Anodize) - Who is Responsible?

krapow

Starting to get Involved
#21
I thought it would be best to give them a chance to address the problem but evidently they do not need our business. We dropped them for their unwillingness to accept ANY responsibility (the consensus of top management here). This decision came after I began this thread.
THE END.
 
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
T Root Cause Failure Analysis - Not following Customer packaging Specification Problem Solving, Root Cause Fault and Failure Analysis 5
Q EU Rep for Packaging waste, WEEE and Battery disposal CE Marking (Conformité Européene) / CB Scheme 0
L AS5553 Clause 3.1.7 e "Control packaging material ..................reused" AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 0
L Packaging unsterile medical devices ISO 13485:2016 - Medical Device Quality Management Systems 6
M MDR - Packaging - Secondary Medical Device Boxes EU Medical Device Regulations 2
Y Packaging validation for non-sterile Medical Equipment Other Medical Device Related Standards 1
M UDI size on packaging EU Medical Device Regulations 3
M UDI placement - Packaging levels EU Medical Device Regulations 2
E Unit Dose Packaging Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 0
B 510(k) clearance claim on medical device product packaging Other US Medical Device Regulations 6
E Packaging Specifications Mercedes-Benz U.S. International IATF 16949 - Automotive Quality Systems Standard 4
TechnicalGuy Colour of symbols on Medical Device labelling and packaging Other Medical Device Related Standards 1
R Labels on sterile packaging EU Medical Device Regulations 5
A Interpretation of Article 16 (2b) - Packaging, samples and Certificate EU Medical Device Regulations 10
I Medical Device Packaging Multilingual Labeling EU Medical Device Regulations 3
N Process Flow diagram steps for inspection and packaging APQP and PPAP 4
C ISO 7010 m002 mandatory action - Color requirements on Packaging IEC 60601 - Medical Electrical Equipment Safety Standards Series 1
shimonv GTIN Number on the Packaging of a Serviced Medical Device EU Medical Device Regulations 0
shimonv Is UDI required on the Packaging of a Serviced/Repaired Medical Device? Other US Medical Device Regulations 3
C QR Code on Medical Device Packaging and Notification to Notified Body EU Medical Device Regulations 1
TheMightyWife Address Change - Medical Device Packaging Labelling Requirements EU Medical Device Regulations 7
E Use of FDA Cleared logo on packaging US Food and Drug Administration (FDA) 8
V Tyvek packaging for Medical device process validation Qualification and Validation (including 21 CFR Part 11) 2
S Symbols - Device label versus Packaging label ISO 13485:2016 - Medical Device Quality Management Systems 1
Y Sterile device packaging under MDR EU Medical Device Regulations 3
A Packaging seal inspection Inspection, Prints (Drawings), Testing, Sampling and Related Topics 2
A Capability Analysis for Packaging Seal Strength with spec. >0.1 Kgf using Minitab Using Minitab Software 6
A Medical Device Class 2A, non sterile bodyworn packaging requirements CE Marking (Conformité Européene) / CB Scheme 7
N Medical device non sterile packaging requirement CE Marking (Conformité Européene) / CB Scheme 1
P Drug packaging / filling operations Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 8
J Animal-Derived products in Packaging Manufacturing and Related Processes 0
P China drug packaging DMF China Medical Device Regulations 0
C ISO 11607-1 Packaging System - Temperature and shipping conditioning Other Medical Device Related Standards 4
M Regulatory intricacies - tertiary packaging of class III MD EU Medical Device Regulations 6
P Secondary packaging operations in medical device facility Manufacturing and Related Processes 1
C Medical Device Packaging Manufacturing - How should product be stored on the pallet 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
Q Does CE Marking include compliance to WEEE and packaging waste? CE Marking (Conformité Européene) / CB Scheme 4
J Biologic Injectable Device Clinical Trial Packaging/Labeling/Artwork Guidelines Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 4
M List of Packaging Contents - Medical Devices - Interpreting EU Directive 93/42/EEC CE Marking (Conformité Européene) / CB Scheme 3
M Does ISO 10993 Apply to Packaging? (e.g. Travel Case) Other Medical Device Related Standards 4
H Require PPAP Before Qualifying Vendor? (Packaging) APQP and PPAP 2
I IATF 8.5.1.5 Requirements c) provision of resources and d) packaging and preservation IATF 16949 - Automotive Quality Systems Standard 1
shimonv Over-Labeling Sterile Packaging - Shelf Life 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
M FDA UDI with Multiple Packaging Configurations Other US Medical Device Regulations 3
shimonv Packaging Validation for Non-Sterile Package EU Medical Device Regulations 4
Pmarszal UDI (Unique Device Identification) Transition Period - Packaging Labeling Other US Medical Device Regulations 5
R Medical Device Packaging Label Validation Other US Medical Device Regulations 8
Pmarszal GUDID Packaging - Two part package Other US Medical Device Regulations 5
J GUDID Labeling and Levels of Packaging 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
R Personalised Food Packaging Training - Internal, External, Online and Distance Learning 2
Similar threads


















































Top Bottom