FDA Inspection 1158748 — Vitalant

Vitalant — FEI 1037368

The FDA completed an inspection of Vitalant on November 22, 2021 in Germantown, 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
November 22, 2021
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Germantown, TN (United States)