FDA Warning Letter — Smith & Nephew Inc.

Case 457814 — FEI 3003604053

The FDA took a Warning Letter action against Smith & Nephew Inc. on April 30, 2015 (Andover, MA). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Smith & Nephew Inc.
Date
April 30, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Andover, MA (United States)