FDA Inspection 735027 — Mayo Clinic Rdrc IRB

Mayo Clinic Rdrc IRB — FEI 2128440

The FDA completed an inspection of Mayo Clinic Rdrc IRB on Jul 19, 2011 in Rochester, MN. 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 19, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Rochester, MN (United States)

Additional Details

Radioactive Drug Research Committee