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FDA Inspection 1041762 — Versiti Blood Center of Wisconsin

Versiti Blood Center of Wisconsin — FEI 1000520116

The FDA completed an inspection of Versiti Blood Center of Wisconsin on November 27, 2017 in Manitowoc, WI. 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
November 27, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Manitowoc, WI (United States)

Facility

Other inspections at this facility

  • 1277835 (NAI Thu Jun 26 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1219496 (NAI Thu Aug 24 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 952444 (NAI Fri Dec 04 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 864420 (NAI Fri Jan 31 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 755566 (NAI Tue Nov 22 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources