FDA Inspection 936680 — AdventHealth Orlando - IRB
The FDA completed an inspection of AdventHealth Orlando - IRB on Jul 30, 2015 in Orlando, FL. 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
- Jul 30, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Orlando, FL (United States)
Additional Details
IRB