FDA Inspection 1261000 — Vitalant

Vitalant — FEI 1000522998

The FDA completed an inspection of Vitalant on Jan 15, 2025 in Grass Valley, 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
Jan 15, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Grass Valley, CA (United States)