Home / Inspections / 933419

FDA Inspection 933419 — Versiti Indiana Inc

Versiti Indiana Inc — FEI 3003103607

The FDA completed an inspection of Versiti Indiana Inc on July 7, 2015 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
July 7, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fishers, IN (United States)

Facility

Other inspections at this facility

  • 1194242 (NAI Wed Dec 07 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 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))
  • 857156 (NAI Mon Dec 02 2013 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