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FDA Inspection
•Erchonia Corporation, LLC•November 24, 2009

Erchonia Corporation, LLC – FDA Inspection, Nov 24, 2009

Record Details

This FDA Inspection record concerns Erchonia Corporation, LLC, with an inspection on November 24, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company
Erchonia Corporation, LLC
Inspection Date
November 24, 2009
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · eda443ff-2093-449f-bdd8-3386f0a3c390

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
630051
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Erchonia Corporation, LLC

7
DateClassificationOfficeProject area
December 14, 2018OAICenter for Devices and Radiological HealthBioresearch Monitoring
October 19, 2018Not classifiedAtlanta District Office
May 16, 2018VAICenter for Devices and Radiological HealthCompliance: Devices
March 12, 2015VAICenter for Devices and Radiological HealthBioresearch Monitoring
September 5, 2012VAICenter for Devices and Radiological HealthRadiation Control and Health Safety Act
View all 7 other inspections on the company page
Other documents for Erchonia Corporation, LLC
  • FDA Inspection 1074668 - 2018-12-14
  • FDA Inspection 1109633 - 2018-10-19
  • FDA Inspection 1052145 - 2018-05-16
  • FDA Inspection 918047 - 2015-03-12
  • FDA Inspection 797366 - 2012-09-05

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