FDA Inspection 639040 — Medtronic, Inc.

Medtronic, Inc. — FEI 2182208

The FDA completed an inspection of Medtronic, Inc. on Jan 22, 2010 in Mounds View, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 22, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Mounds View, MN (United States)