DCX Annual Layout Requirements including Subcomponents

M

michu

#1
Hello,
I've just read DCX customer requirements regarding layout inspection (clause 4.2.6.). Does anybody could give me an interpretaion of following statement (I mean the underline one)
"To ensure continuing conformance to all DC requirements, a complete annual layout including subcomponents, shall be required for all parts"
Does it mean that i should send each componet to laboratory in order to do some material test?
Thanks in advance for your help

michu:thanx:
 
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
K Where do I access DCX Standards referenced in Chrysler Catia notes? Customer and Company Specific Requirements 8
Q Internal Audit Check Lists for GM, Ford, and DCX (TS Specifics) IATF 16949 - Automotive Quality Systems Standard 5
S DCX PSO Part Handling Plan Example Customer and Company Specific Requirements 6
U What evidence would show a TS16949 auditor that you are a DCX Self-Certified Lab? General Auditing Discussions 3
B DCX Product Assurance Testing manual Customer and Company Specific Requirements 3
B DCX Requirement: QA Process Safety and Process Assurance - What are they? Customer and Company Specific Requirements 1
O Supplier Development of Small Suppliers - DCX CSR 4.1.5 Supplier Quality Assurance and other Supplier Issues 1
Q Newest Chrysler DCX PSO Edition? Information about the changes? Customer and Company Specific Requirements 1
M Looking for Chrysler Lay-offs, plant closings, new investments, and other DCX info Customer and Company Specific Requirements 2
M Has anyone made a DCX PSO plant book? Customer and Company Specific Requirements 1
J Need to find past DCX Customer Specific Requirements Customer and Company Specific Requirements 9
M Definition DCX - Can someone tell me what is DCX stands for? DaimlerChrysler? Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 4
M Where can I find a DCX acronym list? Customer and Company Specific Requirements 6
M DaimlerChrysler (DCX) Customer Specific Requirements for PPAP 4th Edition Customer and Company Specific Requirements 8
S Supplier Self certification - DCX Forever Requirements supplement IATF 16949 - Automotive Quality Systems Standard 2
R DCX PSO book 5th Edition - Does anyone have a typical index or check list? APQP and PPAP 6
R DCX S0,S1,S2,V1,what does that mean? Customer and Company Specific Requirements 1
M New DCX Customer Specific Requirements - September 2005 Customer and Company Specific Requirements 1
A EasyMap - Where do I find the software and training for DCX EasyMap Customer and Company Specific Requirements 4
A DCX (Daimler - Chrysler) - PSO (Process Sign-Off) and PAP (Product Planning) Info IATF 16949 - Automotive Quality Systems Standard 9
Q Ppk and Pp on unilateral or unequal tolerance - DCx says Pp can not be calculated Capability, Accuracy and Stability - Processes, Machines, etc. 19
Q First Time Doing Process Sign Off - Tier 2 - DCX - What Do I Need To Know? Customer and Company Specific Requirements 19
K TS 16949 (Ford, DCX, Toyota) Audit of an ISO 17025 (GM Only) In-House Laboratory ISO 17025 related Discussions 2
B DCX (DaimlerChrysler) Customer Specific Requirements July 2004 Customer and Company Specific Requirements 9
I Do I need to sign off my annual audit calendar? Internal Auditing 2
S Annual Inspection Layout - Based on Customer print ? IATF 16949 - Automotive Quality Systems Standard 8
K Updated MSA with the Annual PPAP validations APQP and PPAP 8
T Annual Validation as a detection mode on a PFMEA? FMEA and Control Plans 5
P ISO Class 8 particle count (annual certification vs monitoring) ISO 13485:2016 - Medical Device Quality Management Systems 4
E Annual PPAP+ deviation request ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
A Question on ISO 14001:2015 - Are annual audits required? ISO 14001:2015 Specific Discussions 11
JoCam Increase to bi-annual ISO 13485 audits ISO 13485:2016 - Medical Device Quality Management Systems 2
S Is Annual QMS Training Required? ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 6
M Informational Medicines and Healthcare Products Regulatory Agency Annual Report and Accounts 2018 to 2019 Medical Device and FDA Regulations and Standards News 0
M Informational TGA – Medical device annual reporting – Sponsor obligations Medical Device and FDA Regulations and Standards News 0
S Is an Annual Layout Inspection the same as an Annual Re-validation? Internal Auditing 1
M Informational FDA Invites You to the 2019 Regulatory Education for Industry (REdI) Annual Conference Medical Device and FDA Regulations and Standards News 0
S Post Market Surveillance and Annual Product Review in ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 2
qualprod Annual SWOT for 4.1? I plan to revise quality objectives and strategic route ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
qualprod ISO planning annual meeting? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
JoshuaFroud CDRH Annual Report - eSubmitter Other US Medical Device Regulations 0
B Does anyone charge for annual layouts? APQP and PPAP 8
V How to Add Annual Revalidation requirements to Control Plan? FMEA and Control Plans 5
K Is an annual "audit schedule" the same thing as an audit scope/ audit plan? Internal Auditing 8
S What questions to ask in annual supplier evaluation? ISO 13485:2016 - Medical Device Quality Management Systems 3
M Annual Layout requirements for PPAP/Control Plan FMEA and Control Plans 6
W "On An Annual Basis" - Definition ISO 13485:2016 - Medical Device Quality Management Systems 12
D FDA Guidance Document for Preparing Annual Product Reviews US Food and Drug Administration (FDA) 2
Q FDA - Annual Report Submission Format and QMS updates Other US Medical Device Regulations 2
R Registrar Annual Management Fee Registrars and Notified Bodies 4

Similar threads

Top Bottom