# FDA Inspection 895132 - Syneron, Inc. - September 12, 2014

Source: https://www.keypedia.com/records/fda_inspections/syneron-inc/d2691218-337b-441e-92ad-e5a2f8af267e
Source feed: FDA_Inspections

> FDA Inspection 895132 for Syneron, Inc. on September 12, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 895132
- Company Name: Syneron, Inc.
- Inspection Date: 2014-09-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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