FDA Warning Letter — Smith & Nephew, Inc.

Case 418706 — FEI 3006760724

The FDA took a Warning Letter action against Smith & Nephew, Inc. on Jun 11, 2014 (Saint Petersburg, FL). 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
Jun 11, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Saint Petersburg, FL (United States)