FDA Inspection 884440 — Versiti Indiana, Inc.
The FDA completed an inspection of Versiti Indiana, Inc. on June 24, 2014 in Lafayette, 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
- June 24, 2014
- Fiscal Year
- 2014
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Lafayette, IN (United States)