FDA Inspection 546030 — Medtronic Vascular, Inc.
The FDA completed an inspection of Medtronic Vascular, Inc. on October 9, 2008 in Santa Rosa, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- October 9, 2008
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Santa Rosa, CA (United States)
Additional Details
Sponsor, Contract Research Organization