FDA Inspection 1017177 — AnMed Health System IRB
The FDA completed an inspection of AnMed Health System IRB on Jun 22, 2017 in Anderson, SC. 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
- Jun 22, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Anderson, SC (United States)
Additional details
IRB