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FDA Inspection 597731 — Versiti Illinois, Inc.

Versiti Illinois, Inc. — FEI 1470314

The FDA completed an inspection of Versiti Illinois, Inc. on July 17, 2009 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
July 17, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Winfield, IL (United States)

Facility

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FDA data resources