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FDA Inspection 800754 — Versiti Wisconsin, Inc

Versiti Wisconsin, Inc — FEI 2171378

The FDA completed an inspection of Versiti Wisconsin, Inc on August 10, 2012 in Milwaukee, WI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 10, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Milwaukee, WI (United States)

Facility

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FDA data resources