FDA Inspection 1099392 — Versiti Illinois Inc

Versiti Illinois Inc — FEI 1470340

The FDA completed an inspection of Versiti Illinois Inc on Aug 12, 2019 in Tinley Park, 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
Aug 12, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Tinley Park, IL (United States)

Citations

IDCFRDescription
9821 CFR 606.100(c)Thorough investigations

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