FDA Warning Letter — Medtronic Navigation, Inc.

Case 110669 — FEI 1000517638

The FDA took a Warning Letter action against Medtronic Navigation, Inc. on May 7, 2010 (Lafayette, CO). 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 Navigation, Inc.
Date
May 7, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Lafayette, CO (United States)