FDA Inspection 1062165 — Dentlight Inc

Dentlight Inc — FEI 3005515469

The FDA completed an inspection of Dentlight Inc on August 15, 2018 in Plano, TX. 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 15, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Plano, TX (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
369621 CFR 820.100(b)Documentation