FDA Inspection 958083 — Versiti Illinois Inc

Versiti Illinois Inc — FEI 1000115640

The FDA completed an inspection of Versiti Illinois Inc on Jan 13, 2016 in Highland, IN. 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 13, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Highland, IN (United States)