FDA Inspection 1252448 — Vivos Therapeutics Inc.

Vivos Therapeutics Inc. — FEI 3022315836

The FDA completed an inspection of Vivos Therapeutics Inc. on Oct 24, 2024 in Murray, KY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 24, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Murray, KY (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.