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FDA Inspection 1040708 — Versiti Illinois Inc

Versiti Illinois Inc — FEI 1000115106

The FDA completed an inspection of Versiti Illinois Inc on December 20, 2017 in Westmont, 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
December 20, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Westmont, IL (United States)

Facility

Other inspections at this facility

  • 1274374 (NAI Tue Jun 24 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1170773 (NAI Tue May 24 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 969651 (NAI Thu May 12 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 842691 (NAI Wed Jul 31 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 628597 (NAI Mon Nov 16 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources