FDA Inspection 1238535 — Vitalant

Vitalant — FEI 3003832489

The FDA completed an inspection of Vitalant on May 9, 2024 in Greensburg, 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
May 9, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Greensburg, PA (United States)