Form 483

Kat Implants, LLC Form 483, 2016-04-07

FDA issued a Form 483 to Kat Implants, LLC on 2016-04-07 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

Kat Implants, LLC · Portsmouth, United States · Issued April 7, 2016

Overview

  • 6 public-safe observations are available for this inspection.
  • 6 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.

7 Apr 2016
21 CFR 820.100(b)

Documentation

Cited by Abby E Pelletier

7 Apr 2016
21 CFR 820.198(a)

Complaints

Cited by Abby E Pelletier

7 Apr 2016
21 CFR 820.20(c)

Management review dates

Cited by Abby E Pelletier

7 Apr 2016
21 CFR 820.22

Quality Audits - defined intervals

Cited by Abby E Pelletier

7 Apr 2016
21 CFR 820.70(g)(1)

Maintenance schedule, Lack of or inadequate schedule

Cited by Abby E Pelletier

Inspected site

KIKat Implants, LLCPortsmouth, 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 observations1x
21 CFR 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.20(c)Cited across public-safe Form 483 observations1x
21 CFR 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.70(g)(1)Cited across public-safe Form 483 observations1x
21 CFR 820.90(b)(1)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 6 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