Form 483

Cenorin, LLC Form 483, 2014-05-02

FDA issued a Form 483 to Cenorin, LLC on 2014-05-02 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Cenorin, LLC · Kent, United States · Issued May 2, 2014

Overview

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

2 May 2014
21 CFR 820.30(c)

Design input - documentation

Cited by Sharon I Gundersen

2 May 2014
21 CFR 820.100(b)

Documentation

Cited by Sharon I Gundersen

2 May 2014
21 CFR 820.170(a)

Lack of or inadequate instructions

Cited by Sharon I Gundersen

2 May 2014
21 CFR 820.170(b)

Installer records

Cited by Sharon I Gundersen

Inspected site

CLCenorin, LLCKent, 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 820.170(a)Cited across public-safe Form 483 observations1x
21 CFR 820.170(b)Cited across public-safe Form 483 observations1x
21 CFR 820.30(c)Cited across public-safe Form 483 observations1x

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 4 observations

The source PDF and 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