These regulations implement the FDA's criteria for and authority requiring manufacturers, users and distributors to report health-related medical device failures and their corrections or removal from the market. 21 CFR 803 is an important regulation for devices that may have health-related failures
bag
fda_public
created
Sat, 23 Jun 2012 18:23:00 GMT
creator
dirkjan
modified
Sat, 23 Jun 2012 18:23:00 GMT
modifier
dirkjan
tags
CFR
creator
dirkjan