FDA issued a Warning Letter to Erchonia Corporation on 1/21/2011 for a previous inspection.
483 Erchonia May 2018

483 Erchonia May 2018

Joshua Silvestri FDA$119.00 - Available Now

FDA investigators audited the Erchonia - Melbourne, FL, United States facility and issued inspectional observations (via FDA 483) on 16 May 2018.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 16 May 2018
  • Location: Melbourne, United States
  • FEI: 3003462036
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