FDA Inspection 1167691 — Vitalant

Vitalant — FEI 1771468

The FDA completed an inspection of Vitalant on April 12, 2022 in Rapid City, SD. 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
April 12, 2022
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Rapid City, SD (United States)