FDA Inspection 805484 — Vitalant
The FDA completed an inspection of Vitalant on Oct 31, 2012 in Lewiston, ID. 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 31, 2012
- Fiscal Year
- 2013
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Lewiston, ID (United States)