FDA Inspection 655038 — Versiti Illinois Inc

Versiti Illinois Inc — FEI 1470340

The FDA completed an inspection of Versiti Illinois Inc on Jan 27, 2010 in Tinley Park, 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 27, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Tinley Park, IL (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.