CFG-1003 Form for Dimensional Results - Excel .xls or Word .doc

J

Johan Z

#1
#1
Please help!
Where do I get CFG-1003 (Dimensional Results)?
Preferably as .doc or .xls file

JZ
 
How to manage your QMS while working remotely.
Elsmar Forum Sponsor
Marc

Marc

Hunkered Down for the Duration
Staff member
Admin
#2
#2
It's on page 22 of the PPAP manual. Take 5 minutes and you can put it in excel yourself. There are less than 20 cells to input. The rest is just putting in cell lines. Like I say - 5, maybe 10, minutes at most. Good luck!

BTW, I would use a spreadsheet or a database - not a word processor.
 
A

AnthonyMC

#6
#6
Soooooooooooo... is it too much to expect that there will be a partcertall file with all of the appropriate updates to the 4th edition?

BTW... a great thanks (again) to this place... wonderful, wonderful resource!
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
ncwalker CFG-1003 ..... on steroids - CFG-1003 (like) form that works, and well Excel .xls Spreadsheet Templates and Tools 3
C Strange test result form - CFG-1003 form Inspection, Prints (Drawings), Testing, Sampling and Related Topics 5
V Recording CMM dimensional results on CFG-1003 APQP and PPAP 3
D AIAG PPAP Manual Forms: CFG-1003, CFG-1004, CFG-1005 APQP and PPAP 3
J US Manufacturer of Export Only Exempt Products applying for CFG 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 0
K CFG (certificate of foreign government) Requestor Other US Medical Device Regulations 0
F EU IVD registrations - CFG or CFS - Differences EU Medical Device Regulations 1
M Eligible to obtain certificate of foreign government (CFG) Other Medical Device Regulations World-Wide 15
S Certificate to Foreign Government (CFG) - who is an Exporter ? US Food and Drug Administration (FDA) 2
S CFG Certificate for Medical Device Registration in India Other Medical Device Regulations World-Wide 4
N Foreign Manufacturer requesting FDA's CFG over their country's FSC 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 11
R CFG-type Document for Medical Devices mfg/exported from OUS? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
S FDA Form 3613 [Certificate to Foreign Government (CFG)] - Manufacturer Information 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 14
Michael Malis FDA changed the criteria for Certificate to Foreign Government (CFG) on 12/08/09 US Food and Drug Administration (FDA) 1
M CFG - Certificate for Foreign Government - Medical Device Company based in CA, USA US Food and Drug Administration (FDA) 4
M Updating Certificate of Foreign Government (CFG's) Other US Medical Device Regulations 18
C List of Countries that require 'Certificates to Foreign Governments' (CFG) US Food and Drug Administration (FDA) 4
A Quality Assurance System Evaluation Checklist for AAR M-1003 Other ISO and International Standards and European Regulations 11
B Difference between ISO 9001:2000 and AAR M-1003 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 14
J AAR M-1003 - No design exclusions permitted Design and Development of Products and Processes 4
A AS9102B - 3.6 Design Characteristics and form 3 AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 3
M AS9102 FAI Report formats - Boxes in form 1, 2, 3 of AS9102 AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 4
C AS9145 Appendix D PPAP Approval Form APQP and PPAP 2
L Form-dependent position prevention control FMEA and Control Plans 1
Y Blank Fields on CAPA Form Document Control Systems, Procedures, Forms and Templates 21
Q Do Management Review records have to be on a controlled form? ISO 13485:2016 - Medical Device Quality Management Systems 30
M How to complete structure Analysis and Function analysis sections' columns of AIAG-VDA DFMEA form FMEA and Control Plans 0
P AS9102 Form 3 Dimension Results Inspection, Prints (Drawings), Testing, Sampling and Related Topics 1
M Informational EU – MDCG 2019-12 Designating authority’s final assessment form: Key Information Medical Device and FDA Regulations and Standards News 0
Ed Panek Relevant questions on Substantial Change Form CE Marking (Conformité Européene) / CB Scheme 3
B Documenting hardware on Form 2 of AS9102 AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 5
M Nonconformity for missing form number on the job description document Nonconformance and Corrective Action 1
Sidney Vianna Interesting Discussion Interesting article form the UNIDO Magazine - CSR: a wolf in sheep’s clothing? Sustainability, Green Initiatives and Ecology 16
R Process Specification - What is the name of this PPAP form? APQP and PPAP 15
GreatNate Document Control info - What is required on a controlled form/document for ISO 9001: 2015? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
G I-chart form for GM GP-12 Customer and Company Specific Requirements 2
M Informational US FDA – Ethicon Recalls Circular Staplers for Insufficient Firing and Failure to Completely Form Staples Medical Device and FDA Regulations and Standards News 0
B AS9102 COTS Form 1 vs. 2 AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 5
D Incoming (Receiving) Inspection - General form for incoming part inspection Document Control Systems, Procedures, Forms and Templates 17
S C of C release with accompanying EASA Form 1 for EASA Part 145 EASA and JAA Aviation Standards and Requirements 0
S Where did FDA 510(K) form 3654 go? Other US Medical Device Regulations 1
M What are the differences between "Process Flowchart form" and "Process Flow Diagram form"? IATF 16949 - Automotive Quality Systems Standard 4
K Does anyone have a copy of a GM 5 Phase Problem solving form Problem Solving, Root Cause Fault and Failure Analysis 1
Ron Rompen Source needed for Spline Form gauge (GO and NOGO members) General Measurement Device and Calibration Topics 3
T NAFTA request for form with no part numbers showing Supply Chain Security Management Systems 0
C Do we need to make a new OFI (Opportunity for Improvement) for each document/form we update? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 23
R SaMD - Software as a Medical Device - Software change control form ISO 13485:2016 - Medical Device Quality Management Systems 3
K Work Order Form (Controlled Document)? Document Control Systems, Procedures, Forms and Templates 5
J Medical Device Vigilance decision tree FORM - Please share yours EU Medical Device Regulations 14
O Localized clean room dust extraction system coupled in HVAC - Manufacturing solid dosage form Manufacturing and Related Processes 9
Similar threads
Top Bottom