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FDA Inspection 1036960 — Versiti Wisconsin, Inc

Versiti Wisconsin, Inc — FEI 3004038411

The FDA completed an inspection of Versiti Wisconsin, Inc on December 11, 2017 in La Crosse, 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
December 11, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
La Crosse, WI (United States)

Facility

Other inspections at this facility

  • 1271678 (NAI Wed Apr 16 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1109446 (NAI Wed Oct 30 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 952437 (NAI Tue Dec 15 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 876138 (NAI Fri Apr 25 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 767160 (NAI Fri Feb 10 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources