FDA Inspection 542508 — Medtronic Inc
The FDA completed an inspection of Medtronic Inc on Oct 2, 2008 in Plymouth, 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
- Oct 2, 2008
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Plymouth, MN (United States)
Additional Details
Postmarket Audit Inspections