FDA Inspection 1256872 — Vitalant

Vitalant — FEI 2972352

The FDA completed an inspection of Vitalant on Dec 5, 2024 in Merced, 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
Dec 5, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Merced, CA (United States)