Form 483

Katecho LLC Form 483, 2021-07-16

FDA issued a Form 483 to Katecho LLC on 2021-07-16 with 12 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health12 observations

Katecho LLC · Des Moines, United States · Issued July 16, 2021

Overview

  • 12 public-safe observations are available for this inspection.
  • 4 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.

16 Jul 2021
21 CFR 820.100(b)

Documentation

Cited by Jennifer S Ness, Clifford F Long

16 Jul 2021
21 CFR 820.100(b)

Documentation

Cited by Jennifer S Ness, Clifford F Long

16 Jul 2021
21 CFR 820.100(b)

Documentation

Cited by Jennifer S Ness, Clifford F Long

16 Jul 2021
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Jennifer S Ness, Clifford F Long

16 Jul 2021
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Jennifer S Ness, Clifford F Long

Inspected site

KLKatecho LLCDes Moines, 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 observations3x
21 CFR 820.198(a)Cited across public-safe Form 483 observations3x
21 CFR 820.75(a)Cited across public-safe Form 483 observations3x
21 CFR 820.75(b)Cited across public-safe Form 483 observations3x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 12 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