FDA Inspection 931564 — Amita Health IRB

Amita Health IRB — FEI 3014669549

The FDA completed an inspection of Amita Health IRB on June 23, 2015 in Elk Grove Village, IL. 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
June 23, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Elk Grove Village, IL (United States)

Additional Details

IRB