FDA Inspection 1101259 — Vitalant
The FDA completed an inspection of Vitalant on Jul 15, 2019 in Moses Lake, WA. 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
- Jul 15, 2019
- Fiscal Year
- 2019
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Moses Lake, WA (United States)