FDA Inspection 1180601 — Vitalant

Vitalant — FEI 3014715433

The FDA completed an inspection of Vitalant on Aug 30, 2022 in Spokane, WA. 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
Aug 30, 2022
Fiscal Year
2022
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Spokane, WA (United States)