In the [[FDA Regulations]] a ''Device Master File'' (DMF) means a compilation of records describing the design history of a finished device.


Compare [[Device Master Record]]
bag
fda_public
created
Fri, 03 Aug 2012 14:34:10 GMT
creator
dirkjan
modified
Fri, 03 Aug 2012 14:34:10 GMT
modifier
dirkjan
tags
CFR
CFR 21-820.40
Document Controls
FDA
Quality System Requirements
Term
creator
dirkjan