FDA Inspection 1254409 — Neuronetrix Solutions, LLC

Neuronetrix Solutions, LLC — FEI 3011184129

The FDA completed an inspection of Neuronetrix Solutions, LLC on November 7, 2024 in Louisville, KY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 7, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Louisville, KY (United States)

Citations

IDCFRDescription
2280021 CFR 830.300(a)Devices subject to device identification GUDID data submission requirements.
317021 CFR 820.198(b)Review and evaluation for investigation