FDA Inspection 833390 — Versiti Illinois Inc
The FDA completed an inspection of Versiti Illinois Inc on May 29, 2013 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
- May 29, 2013
- Fiscal Year
- 2013
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Aurora, IL (United States)