FDA Inspection 950998 — Vitalant
The FDA completed an inspection of Vitalant on December 1, 2015 in Lake Bluff, IL. 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
- December 1, 2015
- Fiscal Year
- 2016
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Lake Bluff, IL (United States)