FDA Inspection 1067700 — Versiti Wisconsin, Inc

Versiti Wisconsin, Inc — FEI 2171378

The FDA completed an inspection of Versiti Wisconsin, Inc on Aug 23, 2018 in Milwaukee, 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
Aug 23, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Milwaukee, WI (United States)

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