FDA Inspection 1328280 — Vantis Vascular, Inc

Vantis Vascular, Inc — FEI 3032277090

The FDA completed an inspection of Vantis Vascular, Inc on Jul 23, 2026 in San Jose, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 23, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
San Jose, CA (United States)

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