FDA Inspection 921664 — Versiti Wisconsin, Inc.

Versiti Wisconsin, Inc. — FEI 1000116313

The FDA completed an inspection of Versiti Wisconsin, Inc. on Apr 9, 2015 in West Bend, 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
Apr 9, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
West Bend, WI (United States)

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