# FDA Inspection 1302196 - Ives EEG Solutions, LLC - February 06, 2026

Source: https://www.keypedia.com/records/fda_inspections/ives-eeg-solutions-llc/e77e8706-ccb2-4dd4-a76d-88f2cb1dc1bb
Source feed: FDA_Inspections

> FDA Inspection 1302196 for Ives EEG Solutions, LLC on February 06, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1302196
- Company Name: Ives EEG Solutions, LLC
- Inspection Date: 2026-02-06
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1302196 - 2026-02-06](https://www.keypedia.com/records/fda_inspections/ives-eeg-solutions-llc/976b826c-9cb2-4258-89ad-7440cd94a708)
- [FDA Inspection 1302196 - 2026-02-06](https://www.keypedia.com/records/fda_inspections/ives-eeg-solutions-llc/b7f25a7b-5811-47c1-86e9-700b244f3859)
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- [FDA Inspection 806769 - 2012-10-12](https://www.keypedia.com/records/fda_inspections/ives-eeg-solutions-llc/04080da7-59e0-4165-85b4-f9f8a7bbea14)

Company: https://www.keypedia.com/companies/ives-eeg-solutions-llc/2ffbce65-c855-476e-9086-ee60b122cd70

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7