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FDA Inspection 767160 — Versiti Wisconsin, Inc

Versiti Wisconsin, Inc — FEI 3004038411

The FDA completed an inspection of Versiti Wisconsin, Inc on February 10, 2012 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
February 10, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
La Crosse, WI (United States)

Facility

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