FDA Inspection 1016866 — Cosmedent, Inc.

Cosmedent, Inc. — FEI 1450653

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

Inspection Details

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