Form 483

Kat Implants, LLC Form 483, 2022-09-16

FDA issued a Form 483 to Kat Implants, LLC on 2022-09-16 with 8 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health8 observations

Kat Implants, LLC · Portsmouth, United States · Issued September 16, 2022

Overview

  • 8 public-safe observations are available for this inspection.
  • 2 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.

16 Sep 2022
21 CFR 820.184

DHR - not or inadequately maintained

Cited by Katarzyna Plona

16 Sep 2022
21 CFR 820.184

DHR - not or inadequately maintained

Cited by Katarzyna Plona

16 Sep 2022
21 CFR 820.198(a)

Complaints

Cited by Katarzyna Plona

16 Sep 2022
21 CFR 820.198(a)

Complaints

Cited by Katarzyna Plona

16 Sep 2022
21 CFR 820.184

DHR - not or inadequately maintained

Cited by Katarzyna Plona

Inspected site

KIKat Implants, LLCPortsmouth, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.184Cited across public-safe Form 483 observations4x
21 CFR 820.198(a)Cited across public-safe Form 483 observations4x

Source document

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PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 8 observations

The source PDF, 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