FDA Inspection 1276099 — Vitalant

Vitalant — FEI 1000139516

The FDA completed an inspection of Vitalant on Jun 18, 2025 in Las Cruces, NM. 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
Jun 18, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Las Cruces, NM (United States)

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