FDA Inspection 605963 — Amita Health IRB

Amita Health IRB — FEI 3014669549

The FDA completed an inspection of Amita Health IRB on Aug 17, 2009 in Elk Grove Village, IL. 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
Aug 17, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Elk Grove Village, IL (United States)

Additional details

IRB

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.