FDA Inspection 1233322 — Vitalant

Vitalant — FEI 1000121186

The FDA completed an inspection of Vitalant on March 13, 2024 in Coraopolis, 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
March 13, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Coraopolis, PA (United States)