# Syneron, Inc. - Inspection Records

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

> Inspection records and compliance data for Syneron, Inc. in Irvine, California. Access full analysis and detailed observations.

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## Details

- Name: Syneron, Inc.
- FEI Number: 3004772125
- City: Irvine
- State: California
- Country Name: United States
- Address Line 1: 3 Goodyear Ste A
- Zip Code: 92618

## Related Documents

- [FDA Inspection 1062605 - Syneron, Inc. - 2018-08-15](https://www.keypedia.com/records/fda_inspections/syneron-inc/4c5de985-96f1-4697-85b1-2c08b8cff778) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 15, 2018
- [FDA Inspection 1062605 - Syneron, Inc. - 2018-08-15](https://www.keypedia.com/records/fda_inspections/syneron-inc/4baecbac-5a79-452f-86d1-54e55de771b8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 15, 2018
- [FDA Inspection 895132 - Syneron, Inc. - 2014-09-12](https://www.keypedia.com/records/fda_inspections/syneron-inc/d2691218-337b-441e-92ad-e5a2f8af267e) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2014
- [FDA Inspection 733570 - Syneron, Inc. - 2011-07-05](https://www.keypedia.com/records/fda_inspections/syneron-inc/947fe7c5-628f-4347-807d-df7cc72da9be) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 5, 2011
- [FDA Inspection 733570 - Syneron, Inc. - 2011-07-05](https://www.keypedia.com/records/fda_inspections/syneron-inc/026a6c79-50bb-4503-86fc-23d87a1ee597) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 5, 2011
- [FDA Inspection 675278 - Syneron, Inc. - 2010-08-06](https://www.keypedia.com/records/fda_inspections/syneron-inc/880a2ad0-b7b6-4b11-9c9d-01052d17ef43) — classification: No Action Indicated (NAI), source: FDA, date: August 6, 2010
- [FDA Inspection 675278 - Syneron, Inc. - 2010-08-06](https://www.keypedia.com/records/fda_inspections/syneron-inc/1574c887-cc51-471d-83ed-fe595baa1f64) — classification: Official Action Indicated (OAI), source: FDA, date: August 6, 2010

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