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FDA Inspection 1092594 — UMMC Diagnostic Andrology Lab

UMMC Diagnostic Andrology Lab — FEI 3003980967

The FDA completed an inspection of UMMC Diagnostic Andrology Lab on May 15, 2019 in Minneapolis, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 15, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Minneapolis, MN (United States)

Facility

Other inspections at this facility

  • 1258352 (NAI Mon Jan 13 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 994644 (NAI Tue Dec 13 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 921329 (NAI Wed Apr 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 852202 (NAI Thu Sep 05 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 704641 (NAI Tue Jan 04 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources