FDA Inspection 611880 — UMMC Diagnostic Andrology Lab

UMMC Diagnostic Andrology Lab — FEI 3003980967

The FDA completed an inspection of UMMC Diagnostic Andrology Lab on September 3, 2009 in Minneapolis, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 3, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Minneapolis, MN (United States)

Citations

IDCFRDescription
1222121 CFR 1271.47(a)Procedures for all other requirements