FDA Inspection 1063905 — Versiti Wisconsin, Inc D.B.A. Versiti Blood Center Of Wisconsin

Versiti Wisconsin, Inc D.B.A. Versiti Blood Center Of Wisconsin — FEI 3000717959

The FDA completed an inspection of Versiti Wisconsin, Inc D.B.A. Versiti Blood Center Of Wisconsin on Aug 1, 2018 in Marshfield, 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 1, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Marshfield, WI (United States)

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