FDA Inspection 1265072 — Voom Medical Devices, LLC

Voom Medical Devices, LLC — FEI 3022928161

The FDA completed an inspection of Voom Medical Devices, LLC on Mar 12, 2025 in Brentwood, TN. 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
Mar 12, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Brentwood, TN (United States)

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