DOD First Article Test Plan & Report

GAGEpack - Gage & Calibration Management
Elsmar Forum Sponsor
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
Marc DOD, DHS and NASA Are Driving Adoption of Internet of Things Sensors IEC 27001 - Information Security Management Systems (ISMS) 1
B DIACAP (DoD Information Assurance Certification and Accreditation Process) and CON Various Other Specifications, Standards, and related Requirements 2
apestate Acceptance Sampling - Interpretation of "Lot" - DOD DCMA Inspector coming Inspection, Prints (Drawings), Testing, Sampling and Related Topics 1
apestate Question on wording in DOD RFQ regarding ISO 9000 Various Other Specifications, Standards, and related Requirements 7
apestate At-Source DCMA QAR DOD Inspector finds fault with Part Marking Various Other Specifications, Standards, and related Requirements 5
A DoD Classification of Class 1 and 2 Design Changes and what spec it's called out in Design and Development of Products and Processes 2
Z Department of Defense (DoD) Quality Plan Document Control Systems, Procedures, Forms and Templates 11
R Certificate of compliance (C of C) DOD requirements for commercial items in products Various Other Specifications, Standards, and related Requirements 3
T USAF DoD trained in calibration - Looking for Careerpath advice.... Career and Occupation Discussions 5
ScottK The Berry Amendment (Imposed by 10 U.S.C. 2533a) for DoD parts - Trying to decipher Various Other Specifications, Standards, and related Requirements 7
M Help DOD inspection - Standard temperature calipers should be calibrated at? General Measurement Device and Calibration Topics 7
E Material Review Boards - Are these DOD things a thing of the past? Nonconformance and Corrective Action 14
R APQP and Dod Product Qualification Program (Production Line Qualification) APQP and PPAP 4
Marc Where to find government DoD specifications and standards - Mil Specs Various Other Specifications, Standards, and related Requirements 0
P MDR Article 27 - UDI - Keeping records of UDIs EU Medical Device Regulations 0
K 2021/2226 on Electronic Instructions for Use (IFU) for medical devices Article 22 Packs EU Medical Device Regulations 1
A MDR article 54(2) "modifying" EU Medical Device Regulations 1
B 2017/745 Article 22 EU Medical Device Regulations 6
D AS9100D 8.5.1.3 First Article AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 9
F The meaning of MDR Article 61 6(b) EU Medical Device Regulations 1
S Meaning of Article 61 (10) of the MDR 2017/745 EU Medical Device Regulations 3
A Article 54, Article 61(4) the meaning of marketed device EU Medical Device Regulations 8
L Article 87 Field Safety Corrective Actions in a third country EU Medical Device Regulations 2
A MDR Article 16 Certification of Distributors by a Notified Body? EU Medical Device Regulations 8
C Discus Software for First Article Inspection Inspection, Prints (Drawings), Testing, Sampling and Related Topics 1
A Declaring Conformity with MDR Article 120(3) for an MDD Legacy Device EU Medical Device Regulations 1
M Article 22 - Include statement in procedure pack? EU Medical Device Regulations 1
T API SPEC Q1 Clause 5.6.1.2.C).2) First Article Oil and Gas Industry Standards and Regulations 16
S Summary of safety and clinical performance and Article 120(3) of the MDR EU Medical Device Regulations 4
E Article 17 MDR - (Re-)Processing EU Medical Device Regulations 0
H Article 22 MDR System EU Medical Device Regulations 16
F MDR – Article 120 – Transitional provisions EU Medical Device Regulations 8
H MDR Article 13(c) EU Medical Device Regulations 6
Ed Panek Is anyone familiar with Article 60 Certificate of Free Sale EU Medical Device Regulations 6
Ed Panek Interesting Article Coffee Break and Water Cooler Discussions 1
A Medical First Article - Can it be a Delta? ISO 13485:2016 - Medical Device Quality Management Systems 1
M Addition of IFU on local language by distributor - Article 16? EU Medical Device Regulations 1
briteme4 AS9102 First Article Inspection - do I need a second reviewer and signer? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
S MDR - System and procedure pack article 22 and all sub processes that apply ISO 13485:2016 - Medical Device Quality Management Systems 0
C First Article Inspections - 'how to measure' General Measurement Device and Calibration Topics 11
R EU-MDR Article 9-common specifications Other ISO and International Standards and European Regulations 2
M Examples of Combination Products - MDR Article 1 (8) and MDR Article 1(9) Medical Device and FDA Regulations and Standards News 3
F Component maintenance qualification - Regulation (EU) No 1321/2014 Article 5 EASA and JAA Aviation Standards and Requirements 6
M Vigilance - incident found in an article EU Medical Device Regulations 4
dgrainger Informational MHRA guidance on CE UKNI - Article 5.5 - 2021-02 EU Medical Device Regulations 0
U MDD Article 12/ MDr Article 22 interpretation EU Medical Device Regulations 2
M MDR Article 22 Interpretation EU Medical Device Regulations 3
L EU MDR Article 86 PSUR EU Medical Device Regulations 1
K Article 18: Implant Card and information to be communicated. EU Medical Device Regulations 5
R Requirements for MDR Article 22 Systems EU Medical Device Regulations 1

Similar threads

Top Bottom