FDA Inspection 552511 — Versiti Illinois, Inc.

Versiti Illinois, Inc. — FEI 1470337

The FDA completed an inspection of Versiti Illinois, Inc. on Dec 16, 2008 in Joliet, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 16, 2008
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Joliet, IL (United States)

Citations

IDCFRDescription
15421 CFR 606.160(a)(1)Concurrent documentation