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FDA Inspection 842691 — Versiti Illinois Inc

Versiti Illinois Inc — FEI 1000115106

The FDA completed an inspection of Versiti Illinois Inc on July 31, 2013 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
July 31, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Westmont, IL (United States)

Facility

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FDA data resources