FDA Inspection 1281129 — Vitalant

Vitalant — FEI 2571073

The FDA completed an inspection of Vitalant on September 4, 2025 in Pittsburgh, PA. 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
September 4, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pittsburgh, PA (United States)