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FDA Inspection 993218 — Versiti Illinois, Inc.

Versiti Illinois, Inc. — FEI 1470314

The FDA completed an inspection of Versiti Illinois, Inc. on October 24, 2016 in Winfield, 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
October 24, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Winfield, IL (United States)

Facility

Other inspections at this facility

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  • 913725 (NAI Wed Feb 11 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 816854 (NAI Tue Jan 22 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 722804 (NAI Wed May 04 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources