Form 483

ConMed Corporation Form 483, 2016-02-03

FDA issued a Form 483 to ConMed Corporation on 2016-02-03 with 10 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health10 observations

ConMed Corporation · Utica, United States · Issued February 3, 2016

Overview

  • 10 public-safe observations are available for this inspection.
  • 5 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

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

3 Feb 2016
21 CFR 820.100(b)

Documentation

Cited by Nicholas C Mendiola

3 Feb 2016
21 CFR 820.100(b)

Documentation

Cited by Nicholas C Mendiola

3 Feb 2016
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Nicholas C Mendiola

3 Feb 2016
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Nicholas C Mendiola

3 Feb 2016
21 CFR 820.70(g)(1)

Maintenance schedule, Lack of or inadequate schedule

Cited by Nicholas C Mendiola

Inspected site

CCConMed CorporationUtica, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(b)Cited across public-safe Form 483 observations2x
21 CFR 820.198(a)Cited across public-safe Form 483 observations2x
21 CFR 820.70(g)(1)Cited across public-safe Form 483 observations2x
21 CFR 820.75(a)Cited across public-safe Form 483 observations2x
21 CFR 820.75(c)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 10 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