FDA Inspection 1308782 — Mobia Medical Inc

Mobia Medical Inc — FEI 3012309950

The FDA completed an inspection of Mobia Medical Inc on Mar 19, 2026 in Lakeway, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 19, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Lakeway, TX (United States)

Citations

IDCFRDescription
73121 CFR 803.50(a)(1)Report of Death or Serious Injury

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