Form 483

Cadex Electronics Inc. Form 483, 2011-06-08

FDA issued a Form 483 to Cadex Electronics Inc. on 2011-06-08 with 4 public-safe observations.

483· Form 483 issued4 observations

Cadex Electronics Inc. · Richmond, Canada · Issued June 8, 2011

Overview

  • 4 public-safe observations are available for this inspection.
  • 3 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.

8 Jun 2011
21 CFR 820.30(e)

Design review - documentation

Cited by Amy M Cramer

8 Jun 2011
21 CFR 820.30(e)

Design review - Lack of or inadequate procedures

Cited by Amy M Cramer

8 Jun 2011
21 CFR 820.30(f)

Design verification - output does not meet input requirement

Cited by Amy M Cramer

8 Jun 2011
21 CFR 820.184

DHR content

Cited by Amy M Cramer

Inspected site

CECadex Electronics Inc.Richmond, Canada

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.30(e)Cited across public-safe Form 483 observations2x
21 CFR 820.184Cited across public-safe Form 483 observations1x
21 CFR 820.30(f)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 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