FDA Inspection 1259591 — Brain Tunnelgenix Technologies

Brain Tunnelgenix Technologies — FEI 3008064428

The FDA completed an inspection of Brain Tunnelgenix Technologies on Jan 31, 2025 in Aventura, FL. 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
Jan 31, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Aventura, FL (United States)

Citations

IDCFRDescription
334321 CFR 820.198(e)Maintained