FDA Inspection 1319318 — Vitalant

Vitalant — FEI 1034631

The FDA completed an inspection of Vitalant on May 18, 2026 in Memphis, TN. 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 18, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Memphis, TN (United States)