FDA Inspection
Syneron, Inc.Syneron, Inc. – FDA Inspection, Aug 6, 2010
Record Details
This FDA Inspection record concerns Syneron, Inc., with an inspection on August 6, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Syneron, Inc.
- Inspection Date
- August 6, 2010
- Product Type
- Devices
View Company Profile
ID · 1574c887-cc51-471d-83ed-fe595baa1f64
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 675278
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Syneron, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| August 15, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 12, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 5, 2011 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Syneron, Inc.
- FDA Inspection 1062605 - 2018-08-15
- FDA Inspection 895132 - 2014-09-12
- FDA Inspection 733570 - 2011-07-05
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