FDA Inspection 1265072 — Voom Medical Devices, LLC

Voom Medical Devices, LLC — FEI 3022928161

The FDA completed an inspection of Voom Medical Devices, LLC on March 12, 2025 in New York, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 12, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
New York, NY (United States)