FDA Inspection
Cosmedent, Inc.Cosmedent, Inc. – FDA Inspection, Jun 11, 2009
Record Details
This FDA Inspection record concerns Cosmedent, Inc., with an inspection on June 11, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Cosmedent, Inc.
- Inspection Date
- June 11, 2009
- Product Type
- Devices
View Company Profile
ID · 71b4899a-abb0-47d1-a2fc-0142cd74ff69
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 596468
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.90(a)Specific non-conforming product procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Cosmedent, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| June 7, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 24, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 10, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 10, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Cosmedent, Inc.
- FDA Inspection 1016866 - 2017-06-07
- FDA Inspection 865876 - 2014-02-24
- FDA Inspection 723034 - 2011-03-10
- FDA Inspection 713377 - 2011-03-10
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