FDA Warning Letter — St. Jude Medical

Case 56402 — FEI 2182269

The FDA took a Warning Letter action against St. Jude Medical on April 17, 2009 (Minnetonka, MN). 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
April 17, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Minnetonka, MN (United States)