Form 483

Erchonia Corporation, LLC Form 483, 2018-12-14

FDA issued a Form 483 to Erchonia Corporation, LLC on 2018-12-14 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

Erchonia Corporation, LLC · Melbourne, United States · Issued December 14, 2018

Overview

  • 3 public-safe observations are available for this inspection.
  • 3 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

14 Dec 2018
21 CFR 812.43(c)(5)

No financial disclosure info in investigator agreement

Cited by Stephanie C Mangigian, Kelly N Kerr

14 Dec 2018
21 CFR 812.46(a)

Sponsor securing investigator compliance

Cited by Stephanie C Mangigian, Kelly N Kerr

14 Dec 2018
21 CFR 812.40

Sponsors' general responsibilities

Cited by Stephanie C Mangigian, Kelly N Kerr

Inspected site

ECErchonia Corporation, LLCMelbourne, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 812.40Cited across public-safe Form 483 observations1x
21 CFR 812.43(c)(5)Cited across public-safe Form 483 observations1x
21 CFR 812.46(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 3 observations

Every observation in full, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere