# FDA Inspection 1324380 - NeuroVention, LLC - June 23, 2026

Source: https://www.keypedia.com/records/fda_inspections/neurovention-llc/4c1cb894-5a99-420d-a342-339f09dcb2e5
Source feed: FDA_Inspections

> FDA Inspection 1324380 for NeuroVention, LLC on June 23, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1324380
- Company Name: NeuroVention, LLC
- Inspection Date: 2026-06-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1206678 - 2023-05-31](https://www.keypedia.com/records/fda_inspections/neurovention-llc/5c2ee510-822c-4384-bd27-c9c16951f1cf)
- [FDA Inspection 1206678 - 2023-05-31](https://www.keypedia.com/records/fda_inspections/neurovention-llc/d5522d2c-5718-4872-8723-c6011a66c1a5)

Company: https://www.keypedia.com/companies/neurovention-llc/557599ec-5ae1-4290-bfab-ebf182abaa73

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