# FDA Inspection 1180641 - BIOSONIX - September 22, 2022

Source: https://www.keypedia.com/records/fda_inspections/biosonix/18b78b49-fee0-4cfb-95d8-189a58c5f2a0
Source feed: FDA_Inspections

> FDA Inspection 1180641 for BIOSONIX on September 22, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1180641
- Company Name: BIOSONIX
- Inspection Date: 2022-09-22
- 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 1180641 - 2022-09-22](https://www.keypedia.com/records/fda_inspections/biosonix/57d0b055-f05d-44f8-b3c3-2e4efd98b77f)

Company: https://www.keypedia.com/companies/biosonix/30f3699e-093a-46bc-856e-5b64815be3db

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