FDA Inspection 1199067 — Vitalant

Vitalant — FEI 2971465

The FDA completed an inspection of Vitalant on February 24, 2023 in Reno, NV. 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
February 24, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Reno, NV (United States)