483 RESPONSE
Biomet, Inc.FDA 483_RESPONSE - Biomet, Inc. - November 22, 2016
Discuss this record with AI
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.
Record Details
This 483 RESPONSE record concerns Biomet, Inc., with an inspection on November 22, 2016, issued by the Office of Health Technology 5 (Neurological and Physical Medicine Devices), covering devices.
Open in Dashboard
ID · 159e464e-90ad-4ff9-a4d7-e4c8086af1be
Violation Codes3
21 CFR 82021 CFR 820.5FD&C Act 801(a)(3)
Full citation text and observation details available on the Dashboard.