# Ives EEG Solutions, LLC – FDA Inspection, Mar 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/ives-eeg-solutions-llc/b0a63b36-ed8a-4ef4-8b26-707f902dd168
Source feed: FDA_Inspections

> FDA inspection 1004457 of Ives EEG Solutions, LLC, March 23, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1004457
- Company Name: Ives EEG Solutions, LLC
- Inspection Date: 2017-03-23
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1302196 - 2026-02-06
- FDA Inspection 1179579 - 2022-09-08
- FDA Inspection 806769 - 2012-10-12

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/nabil-nakhoul/d676e9c9-566c-4e59-84e8-1dc474e4e48d)

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
