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FDA Inspection 629638 — Versiti Indiana Inc

Versiti Indiana Inc — FEI 3003103607

The FDA completed an inspection of Versiti Indiana Inc on November 10, 2009 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
November 10, 2009
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fishers, IN (United States)

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))
  • 857156 (NAI Mon Dec 02 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources