FDA Inspection 938498 — Andrew S. Wagner, M.D.
The FDA completed an inspection of Andrew S. Wagner, M.D. on August 11, 2015 in Saginaw, MI. 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
- August 11, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Saginaw, MI (United States)
Additional Details
Clinical Investigator (CI)