FDA Warning Letter — DePuy Orthopaedics, Inc.

Case 202552 — FEI 1818910

The FDA took a Warning Letter action against DePuy Orthopaedics, Inc. on December 8, 2011 (Warsaw, IN). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
DePuy Orthopaedics, Inc.
Date
December 8, 2011
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Warsaw, IN (United States)