These regulations implement the FDA's responsibilities and authority to require the recall of failed, defected, adulterated, or misbranded medical devices.

Based on FDA assessment, this regulation empowers the agency with significant powers to remove, through a variety of recall actions, devices the agency feels require removal from the marketplace.
bag
fda_public
created
Sat, 23 Jun 2012 14:58:07 GMT
creator
dirkjan
modified
Sat, 23 Jun 2012 14:58:07 GMT
modifier
dirkjan
tags
CFR
creator
dirkjan