FDA Warning Letter — Medtronic MiniMed, Inc.

Case 617539 — FEI 3003166194

The FDA took a Warning Letter action against Medtronic MiniMed, Inc. on December 9, 2021 (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
December 9, 2021
Fiscal Year
2022
Product Type
Devices
Center
CDRH
Location
Northridge, CA (United States)