FDA Warning Letter — Medtronic, Inc.

Case 560736 — FEI 2182208

The FDA took a Warning Letter action against Medtronic, Inc. on July 30, 2018 (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
July 30, 2018
Fiscal Year
2018
Product Type
Devices
Center
CDRH
Location
Mounds View, MN (United States)