FDA Inspection 885442 — Septodont Inc.

Septodont Inc. — FEI 1721729

The FDA completed an inspection of Septodont Inc. on May 19, 2014 in Louisville, 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
May 19, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Louisville, CO (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
316821 CFR 820.198(a)Complaints