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FDA Inspection 913725 — Versiti Illinois, Inc.

Versiti Illinois, Inc. — FEI 1470314

The FDA completed an inspection of Versiti Illinois, Inc. on February 11, 2015 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
February 11, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Winfield, IL (United States)

Facility

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FDA data resources