FDA Inspection 860388 — Versiti Indiana, Inc
The FDA completed an inspection of Versiti Indiana, Inc on Dec 27, 2013 in Terre Haute, 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
- Dec 27, 2013
- Fiscal Year
- 2014
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Terre Haute, IN (United States)