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FDA Inspection 969651 — Versiti Illinois Inc

Versiti Illinois Inc — FEI 1000115106

The FDA completed an inspection of Versiti Illinois Inc on May 12, 2016 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
May 12, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Westmont, IL (United States)

Facility

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  • 1040708 (NAI Wed Dec 20 2017 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