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FDA Inspection 952444 — Versiti Blood Center Of Wisconsin

Versiti Blood Center Of Wisconsin — FEI 1000520116

The FDA completed an inspection of Versiti Blood Center Of Wisconsin on Dec 4, 2015 in Manitowoc, 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
Dec 4, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Manitowoc, WI (United States)

Facility

Other inspections at this facility

FDA data resources

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