Form 483

Cleartooth Electronics, Inc. Form 483, 2022-04-19

FDA issued a Form 483 to Cleartooth Electronics, Inc. on 2022-04-19 with 20 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health20 observations

Cleartooth Electronics, Inc. · Boulder, United States · Issued April 19, 2022

Overview

  • 20 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.

19 Apr 2022
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Christine I Shaw

19 Apr 2022
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Christine I Shaw

19 Apr 2022
21 CFR 820.30(h)

Design transfer - Lack of or inadequate procedures

Cited by Christine I Shaw

19 Apr 2022
21 CFR 820.30(h)

Design transfer - Lack of or inadequate procedures

Cited by Christine I Shaw

19 Apr 2022
21 CFR 820.30(i)

Design changes - Lack of or Inadequate Procedures

Cited by Christine I Shaw

Inspected site

CECleartooth Electronics, Inc.Boulder, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.198(a)Cited across public-safe Form 483 observations4x
21 CFR 820.30(h)Cited across public-safe Form 483 observations4x
21 CFR 820.30(i)Cited across public-safe Form 483 observations4x
21 CFR 820.40Cited across public-safe Form 483 observations4x
21 CFR 820.70(i)Cited across public-safe Form 483 observations4x

Full 483 report

Get the verbatim text of all 20 observations

The full inspection record, as Atlas holds it, 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