FDA Inspection 1043126 — Versiti Illinois, Inc.

Versiti Illinois, Inc. — FEI 1471716

The FDA completed an inspection of Versiti Illinois, Inc. on Jan 25, 2018 in Elgin, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 25, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Elgin, IL (United States)