FDA Inspection 1341882 — Vitalant

Vitalant — FEI 1421612

The FDA completed an inspection of Vitalant on Oct 15, 2026 in Arlington Heights, IL. 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
Oct 15, 2026
Fiscal Year
2027
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Arlington Heights, IL (United States)

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