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FDA Inspection 1040718 — Versiti Indiana, Inc

Versiti Indiana, Inc — FEI 1876566

The FDA completed an inspection of Versiti Indiana, Inc on December 27, 2017 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, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Terre Haute, IN (United States)

Facility

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  • 955785 (NAI Mon Dec 07 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 860388 (NAI Fri Dec 27 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 771124 (NAI Mon Mar 05 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources