# FDA Inspection 1024832 - Vivos Therapeutics, Inc. - September 11, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/vivos-therapeutics-inc/c0625972-7619-4a82-96ca-3f7a7399c8f2
Source feed: FDA_Inspections

> FDA Inspection 1024832 for Vivos Therapeutics, Inc. on September 11, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024832
- Company Name: Vivos Therapeutics, Inc.
- Inspection Date: 2017-09-11
- 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 1127853 - 2020-08-27](https://www.globalkeysolutions.net/records/fda_inspections/vivos-therapeutics-inc/fb5b2ace-2085-44ae-b7e9-9d18c1ff2cc2)
- [FDA Inspection 1024832 - 2017-09-11](https://www.globalkeysolutions.net/records/fda_inspections/vivos-therapeutics-inc/d556fcb5-c0d6-4307-8206-7a6d791fc4b9)

Company: https://www.globalkeysolutions.net/companies/vivos-therapeutics-inc/1caa9650-0b6e-4db3-88b2-79cfd180b012

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