FDA Inspection 720369 — St. Agnes Medical Center IRB

St. Agnes Medical Center IRB — FEI 3008553935

The FDA completed an inspection of St. Agnes Medical Center IRB on Apr 14, 2011 in Fresno, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 14, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Fresno, CA (United States)

Additional Details

IRB