FDA Inspection 1088441 — Vitalant
The FDA completed an inspection of Vitalant on May 1, 2019 in Auburn, CA. 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
- May 1, 2019
- Fiscal Year
- 2019
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Auburn, CA (United States)