FDA Inspection 596468 — Cosmedent, Inc.

Cosmedent, Inc. — FEI 1450653

The FDA completed an inspection of Cosmedent, Inc. on Jun 11, 2009 in Chicago, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 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

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