Syneron, Inc.

Form 483

Irvine, California, United StatesFEI 3004772125Issued July 05, 2011

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3004772125.

Observations6

Issue DateJuly 05, 2011

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Syneron, Inc.
Location: Irvine, California, United States
FEI Number: 3004772125
Product Type: Devices
Issue Date: July 05, 2011
Country: United States

Inspection History, 2010 to 2018

NAI1

VAI2

OAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

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Syneron, Inc. FDA Form 483, Irvine, California, July 5, 2011