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FDA Inspection 1085187 — Versiti Illinois, Inc.

Versiti Illinois, Inc. — FEI 1470314

The FDA completed an inspection of Versiti Illinois, Inc. on March 19, 2019 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
March 19, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Winfield, IL (United States)

Facility

Other inspections at this facility

  • 1197253 (NAI Fri Feb 03 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 993218 (NAI Mon Oct 24 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 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