FDA issued a Warning Letter to Syneron, Inc on 12/23/2010 for a previous inspection.
483 Syneron Jul 2011

483 Syneron Jul 2011

Herminio Francisco FDA$119.00 - Available Now

FDA investigators audited the Syneron - Irvine, CA, United States facility and issued inspectional observations (via FDA 483) on 05 Jul 2011.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 05 Jul 2011
  • Location: Irvine, United States
  • FEI: 3004772125
Add To Cart