FDA issued a Warning Letter to Erchonia Corporation on 1/21/2011 as a result of this inspection.
483 Erchonia Nov 2009

483 Erchonia Nov 2009

$119 - Not in Stock

FDA investigators audited the Erchonia - Melbourne, FL, United States facility and issued inspectional observations (via FDA 483) on 24 Nov 2009.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 24 Nov 2009
  • Location: Melbourne, United States
  • FEI: 3003462036

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