FDA Inspection 1256968 — Vitalant

Vitalant — FEI 2077800

The FDA completed an inspection of Vitalant on December 6, 2024 in San Luis Obispo, CA. 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 6, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Luis Obispo, CA (United States)