FDA Inspection 1198726 — Vitalant

Vitalant — FEI 1000123788

The FDA completed an inspection of Vitalant on February 22, 2023 in Carson City, 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 22, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Carson City, NV (United States)