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FDA Inspection 885386 — Versiti Illinois Inc

Versiti Illinois Inc — FEI 3008393297

The FDA completed an inspection of Versiti Illinois Inc on June 30, 2014 in Bloomingdale, IL. 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
June 30, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bloomingdale, IL (United States)

Facility

Other inspections at this facility

  • 1253952 (NAI Wed Nov 06 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1106928 (NAI Tue Sep 17 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1025428 (NAI Tue Aug 22 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 953249 (NAI Wed Dec 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 696167 (NAI Tue Nov 02 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources