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FDA Inspection 642483 — Versiti Wisconsin, Inc

Versiti Wisconsin, Inc — FEI 3004038411

The FDA completed an inspection of Versiti Wisconsin, Inc on January 26, 2010 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
January 26, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
La Crosse, WI (United States)

Facility

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