FDA Warning Letter — Medtronic MiniMed, Inc.

Case 405884 — FEI 3003166194

The FDA took a Warning Letter action against Medtronic MiniMed, Inc. on September 19, 2013 (Northridge, CA). 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 MiniMed, Inc.
Date
September 19, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Northridge, CA (United States)