FDA Inspection 1309894 — Vitalant

Vitalant — FEI 1000123788

The FDA completed an inspection of Vitalant on Mar 25, 2026 in Carson City, NV. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 25, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Carson City, NV (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.