FDA Warning Letter — Medtronic, Inc.

Case 83764 — FEI 2182208

The FDA took a Warning Letter action against Medtronic, Inc. on November 9, 2009 (Mounds View, 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
Medtronic, Inc.
Date
November 9, 2009
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Mounds View, MN (United States)