FDA Inspection 838096 — Mayo Clinic Rochester

Mayo Clinic Rochester — FEI 3003406951

The FDA completed an inspection of Mayo Clinic Rochester on Jun 27, 2013 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: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 27, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Rochester, MN (United States)