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FDA Inspection 857156 — Versiti Indiana Inc

Versiti Indiana Inc — FEI 3003103607

The FDA completed an inspection of Versiti Indiana Inc on December 2, 2013 in Fishers, 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 2, 2013
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fishers, IN (United States)

Facility

Other inspections at this facility

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  • 1086183 (NAI Thu Apr 04 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1007628 (NAI Tue Mar 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 933419 (NAI Tue Jul 07 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 752847 (NAI Thu Nov 03 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources