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FDA Inspection 1088129 — Versiti Wisconsin, Inc

Versiti Wisconsin, Inc — FEI 2177747

The FDA completed an inspection of Versiti Wisconsin, Inc on March 19, 2019 in Waukesha, 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
March 19, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Waukesha, WI (United States)

Facility

Other inspections at this facility

  • 1236826 (NAI Mon Apr 22 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1003836 (NAI Wed Feb 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 914912 (NAI Wed Feb 18 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 805208 (VAI Fri Oct 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 709944 (NAI Thu Feb 17 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources