FDA Inspection 1127853 — Vivos Therapeutics, Inc.

Vivos Therapeutics, Inc. — FEI 3013530385

The FDA completed an inspection of Vivos Therapeutics, Inc. on August 27, 2020 in Littleton, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 27, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Littleton, CO (United States)

Citations

IDCFRDescription
310421 CFR 820.30(j)Design history file
313021 CFR 820.100(a)Lack of or inadequate procedures