FDA Inspection 1236651 — Versiti Wisconsin, Inc.

Versiti Wisconsin, Inc. — FEI 1000116313

The FDA completed an inspection of Versiti Wisconsin, Inc. on Apr 22, 2024 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 22, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
West Bend, WI (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.