FDA Warning Letter — Synthes, Inc.

Case 239794 — FEI 3005180112

The FDA took a Warning Letter action against Synthes, Inc. on February 16, 2012 (West Chester, PA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Synthes, Inc.
Date
February 16, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
West Chester, PA (United States)