# Syneron, Inc. – FDA Inspection, Aug 15, 2018

Source: https://www.keypedia.com/records/fda_inspections/syneron-inc/4c5de985-96f1-4697-85b1-2c08b8cff778
Source feed: FDA_Inspections

> FDA inspection 1062605 of Syneron, Inc., August 15, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1062605
- Company Name: Syneron, Inc.
- Inspection Date: 2018-08-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 895132 - 2014-09-12
- [FDA Inspection 733570 - 2011-07-05](https://www.keypedia.com/records/fda_inspections/syneron-inc/947fe7c5-628f-4347-807d-df7cc72da9be)
- [FDA Inspection 675278 - 2010-08-06](https://www.keypedia.com/records/fda_inspections/syneron-inc/1574c887-cc51-471d-83ed-fe595baa1f64)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/kelvin-cheung/ded61aee-4b4b-4049-a67c-19d971475be7)

Company: https://www.keypedia.com/companies/syneron-inc/29dd4332-40fd-4266-83a9-82aaa92eb4f3

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7