FDA Inspection 771124 — Versiti Indiana, Inc
The FDA completed an inspection of Versiti Indiana, Inc on Mar 5, 2012 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
- Mar 5, 2012
- Fiscal Year
- 2012
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Terre Haute, IN (United States)