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FDA Inspection 772491 — Versiti Illinois Inc

Versiti Illinois Inc — FEI 3005010959

The FDA completed an inspection of Versiti Illinois Inc on February 28, 2012 in Dekalb, 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
February 28, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Dekalb, IL (United States)

Facility

Other inspections at this facility

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  • 1025429 (NAI Mon Aug 28 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 916787 (NAI Thu Mar 05 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 855918 (NAI Tue Oct 29 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources