FDA Inspection 1160529 — Vitalant

Vitalant — FEI 3000204270

The FDA completed an inspection of Vitalant on December 14, 2021 in Midland, TX. 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
December 14, 2021
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Midland, TX (United States)