FDA Inspection 718005 — Essentia Health IRB #1
The FDA completed an inspection of Essentia Health IRB #1 on March 25, 2011 in Duluth, MN. 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
- March 25, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Duluth, MN (United States)
Additional Details
IRB