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FDA Inspection 860388 — Versiti Indiana, Inc

Versiti Indiana, Inc — FEI 1876566

The FDA completed an inspection of Versiti Indiana, Inc on December 27, 2013 in Terre Haute, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 27, 2013
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Terre Haute, IN (United States)

Facility

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FDA data resources