FDA Inspection 576544 — Mayo Clinic IRB

Mayo Clinic IRB — FEI 2182468

The FDA completed an inspection of Mayo Clinic IRB on April 13, 2009 in Rochester, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 13, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Rochester, MN (United States)

Additional Details

IRB