FDA Inspection 767160 — Versiti Wisconsin, Inc

Versiti Wisconsin, Inc — FEI 3004038411

The FDA completed an inspection of Versiti Wisconsin, Inc on Feb 10, 2012 in La Crosse, 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
Feb 10, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
La Crosse, WI (United States)

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