FDA Inspection 1302196 — Ives EEG Solutions, LLC

Ives EEG Solutions, LLC — FEI 3008806011

The FDA completed an inspection of Ives EEG Solutions, LLC on February 6, 2026 in Newburyport, MA. 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
February 6, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Newburyport, MA (United States)