FDA Inspection 544712 — Vitalant
The FDA completed an inspection of Vitalant on Oct 29, 2008 in Lake Bluff, 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
- Oct 29, 2008
- Fiscal Year
- 2009
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Lake Bluff, IL (United States)