FDA Inspection 853830 — Medtronic, Inc.

Medtronic, Inc. — FEI 2182208

The FDA completed an inspection of Medtronic, Inc. on October 31, 2013 in Mounds View, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 31, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Mounds View, MN (United States)

Additional Details

Sponsor, Contract Research Organization