FDA Inspection 870253 — Olmsted Medical Group IRB

Olmsted Medical Group IRB — FEI 3000718527

The FDA completed an inspection of Olmsted Medical Group IRB on Mar 11, 2014 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
Mar 11, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Rochester, MN (United States)

Additional Details

IRB