Home / Inspections / 628597

FDA Inspection 628597 — Versiti Illinois Inc

Versiti Illinois Inc — FEI 1000115106

The FDA completed an inspection of Versiti Illinois Inc on November 16, 2009 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
November 16, 2009
Fiscal Year
2010
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))
  • 1040708 (NAI Wed Dec 20 2017 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))

FDA data resources