FDA Injunction — Medtronic Neuromodulation

Case 252 — FEI 2182207

The FDA took a Injunction action against Medtronic Neuromodulation on April 29, 2015 (Minneapolis, 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 Neuromodulation
Date
April 29, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Minneapolis, MN (United States)