FDA Warning Letter — DePuy Orthopaedics, Inc.

Case 93167 — FEI 1818910

The FDA took a Warning Letter action against DePuy Orthopaedics, Inc. on August 19, 2010 (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
August 19, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Warsaw, IN (United States)