# FDA Inspection 1118298 - NEXALIN TECHNOLOGY INC. - February 20, 2020

Source: https://www.keypedia.com/records/fda_inspections/nexalin-technology-inc/0a418bfc-8f19-4513-b636-e2f600114db3
Source feed: FDA_Inspections

> FDA Inspection 1118298 for NEXALIN TECHNOLOGY INC. on February 20, 2020. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1118298
- Company Name: NEXALIN TECHNOLOGY INC.
- Inspection Date: 2020-02-20
- 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 1118298 - 2020-02-20](https://www.keypedia.com/records/fda_inspections/nexalin-technology-inc/9656272f-1ce5-4819-9a8d-68597f3cd022)

Company: https://www.keypedia.com/companies/nexalin-technology-inc/3cda8b7b-b766-4b8a-aa59-6f8cec791005

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