FDA Warning Letter — Vivos Therapeutics, Inc.

Case 540821 — FEI 3013530385

The FDA took a Warning Letter action against Vivos Therapeutics, Inc. on Jan 12, 2018 (Littleton, CO). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action details

Facility
Vivos Therapeutics, Inc.
Date
Jan 12, 2018
Fiscal Year
2018
Product Type
Devices
Center
CDRH
Location
Littleton, CO (United States)

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