FDA Inspection 921664 — Versiti Wisconsin, Inc.

Versiti Wisconsin, Inc. — FEI 1000116313

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