FDA Inspection 819376 — Medtronic Vascular, Inc.
The FDA completed an inspection of Medtronic Vascular, Inc. on February 22, 2013 in Santa Rosa, CA. 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
- February 22, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Santa Rosa, CA (United States)
Additional Details
Postmarket Audit Inspections