FDA Inspection 952598 — Versiti Illinois Inc
The FDA completed an inspection of Versiti Illinois Inc on Dec 9, 2015 in Aurora, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Dec 9, 2015
- Fiscal Year
- 2016
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Aurora, IL (United States)