FDA Inspection 1016866 — Cosmedent, Inc.

Cosmedent, Inc. — FEI 1450653

The FDA completed an inspection of Cosmedent, Inc. on Jun 7, 2017 in Chicago, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jun 7, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Chicago, IL (United States)

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