FDA Inspection 628597 — Versiti Illinois Inc
The FDA completed an inspection of Versiti Illinois Inc on Nov 16, 2009 in Westmont, IL. 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
- Nov 16, 2009
- Fiscal Year
- 2010
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Westmont, IL (United States)