FDA Inspection 1102328 — Vitalant

Vitalant — FEI 2577645

The FDA completed an inspection of Vitalant on June 24, 2019 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
June 24, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pittsburgh, PA (United States)