FDA Inspection 1199227 — Vitalant

Vitalant — FEI 1671458

The FDA completed an inspection of Vitalant on February 23, 2023 in Lubbock, 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
February 23, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Lubbock, TX (United States)