FDA Warning Letter — St. Jude Medical

Case 480398 — FEI 3004936110

The FDA took a Warning Letter action against St. Jude Medical on September 30, 2015 (Atlanta, GA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
St. Jude Medical
Date
September 30, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Atlanta, GA (United States)