FDA Inspection
Market Technologies Inc. DBA DermavistaMarket Technologies Inc. DBA Dermavista – FDA Inspection, Jun 19, 2014
Record Details
This FDA Inspection record concerns Market Technologies Inc. DBA Dermavista, with an inspection on June 19, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- June 19, 2014
- Product Type
- Devices
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ID · f0191eec-82f0-4e74-8702-1ef0ca887725
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 882804
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
5- 21 CFR 820.198(a)Complaints
- 21 CFR 820.20(c)Management review - defined interval, sufficient frequency
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.22Quality Audit/Reaudit - conducted
- 21 CFR 803.40(a)Report of death, injury
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Other FDA inspections of Market Technologies Inc. DBA Dermavista
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 4, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 9, 2013 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Market Technologies Inc. DBA Dermavista
- FDA Inspection 905841 - 2014-12-04
- FDA Inspection 829188 - 2013-05-09
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