FDA Inspection 642483 — Versiti Wisconsin, Inc

Versiti Wisconsin, Inc — FEI 3004038411

The FDA completed an inspection of Versiti Wisconsin, Inc on Jan 26, 2010 in La Crosse, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jan 26, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
La Crosse, WI (United States)

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