FDA Inspection 1205605 — Vitalant

Vitalant — FEI 1000143480

The FDA completed an inspection of Vitalant on May 4, 2023 in Aberdeen, SD. 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 4, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Aberdeen, SD (United States)