FDA Inspection 1180596 — Vitalant

Vitalant — FEI 3017723002

The FDA completed an inspection of Vitalant on Sep 8, 2022 in Greeley, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 8, 2022
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Greeley, CO (United States)