# FDA Inspection 1252882 - NeuroOne Medical Technologies Corporation - October 28, 2024

Source: https://www.keypedia.com/records/fda_inspections/neuroone-medical-technologies-corporation/1ad370d8-ece1-4ac3-b0b5-64b944862b30
Source feed: FDA_Inspections

> FDA Inspection 1252882 for NeuroOne Medical Technologies Corporation on October 28, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1252882
- Company Name: NeuroOne Medical Technologies Corporation
- Inspection Date: 2024-10-28
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Minneapolis District Office

## Related Documents

- [FDA Inspection 1252882 - 2024-10-28](https://www.keypedia.com/records/fda_inspections/neuroone-medical-technologies-corporation/5104293c-4eae-49d7-bd47-64818a4ee132)
- [FDA Inspection 1252882 - 2024-10-28](https://www.keypedia.com/records/fda_inspections/neuroone-medical-technologies-corporation/6057e279-0ad9-41d1-9f6a-2598fd96dacf)
- [FDA Inspection 1252882 - 2024-10-28](https://www.keypedia.com/records/fda_inspections/neuroone-medical-technologies-corporation/c29d37c5-4acc-442e-b787-0fd34b14923e)
- [FDA Inspection 1159398 - 2021-12-16](https://www.keypedia.com/records/fda_inspections/neuroone-medical-technologies-corporation/291df6df-e1c5-480a-9528-c2988483e37e)

Company: https://www.keypedia.com/companies/neuroone-medical-technologies-corporation/9b0d5e64-3353-43e0-83b5-8383d1545cb5

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d