FDA Inspection 1237997 — Vitalant

Vitalant — FEI 1000523276

The FDA completed an inspection of Vitalant on March 27, 2024 in Napa, CA. 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
March 27, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Napa, CA (United States)