# FDA Inspection 1047611 - Sonendo Inc - March 23, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/sonendo-inc/d9695820-e8bd-429f-ab82-b1fed10e6a97
Source feed: FDA_Inspections

> FDA Inspection 1047611 for Sonendo Inc on March 23, 2018. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1047611
- Company Name: Sonendo Inc
- Inspection Date: 2018-03-23
- 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 1047611 - 2018-03-23](https://www.globalkeysolutions.net/records/fda_inspections/sonendo-inc/546126d3-329e-41e6-a2f0-98e5baec9c82)
- [FDA Inspection 981507 - 2016-02-26](https://www.globalkeysolutions.net/records/fda_inspections/sonendo-inc/64d1656c-6e68-407d-bb8a-412df9713ae9)
- [FDA Inspection 981507 - 2016-02-26](https://www.globalkeysolutions.net/records/fda_inspections/sonendo-inc/dacdec1f-2694-4216-bfbd-7a67a8675445)

Company: https://www.globalkeysolutions.net/companies/sonendo-inc/334931d8-d0d3-4c65-ba66-94d0cc6b43d0

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