FDA Inspection 802838 — Medtronic Navigation, Inc.
The FDA completed an inspection of Medtronic Navigation, Inc. on September 6, 2012 in Lafayette, CO. 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
- September 6, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Lafayette, CO (United States)