FDA Inspection 596468 — Cosmedent, Inc.

Cosmedent, Inc. — FEI 1450653

The FDA completed an inspection of Cosmedent, Inc. on June 11, 2009 in Chicago, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 11, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Chicago, IL (United States)

Citations

IDCFRDescription
328321 CFR 820.90(a)Specific non-conforming product procedures