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FDA Inspection 952437 — Versiti Wisconsin, Inc

Versiti Wisconsin, Inc — FEI 3004038411

The FDA completed an inspection of Versiti Wisconsin, Inc on December 15, 2015 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 15, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
La Crosse, WI (United States)

Facility

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  • 1036960 (NAI Mon Dec 11 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 876138 (NAI Fri Apr 25 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources