FDA Inspection 1122848 — Versiti Indiana, Inc

Versiti Indiana, Inc — FEI 1876566

The FDA completed an inspection of Versiti Indiana, Inc on March 16, 2020 in Terre Haute, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 16, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Terre Haute, IN (United States)