Form 483

Agilent Technologies, Inc Form 483, 2009-04-14

FDA issued a Form 483 to Agilent Technologies, Inc on 2009-04-14 with 3 public-safe observations.

483· Form 483 issued3 observations

Agilent Technologies, Inc · Winooski, United States · Issued April 14, 2009

Overview

  • 3 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.

14 Apr 2009
21 CFR 803.50(a)(2)

Report of Malfunction

Cited by Laurie B Frazier

14 Apr 2009
21 CFR 820.30(g)

Design Validation - Risk analysis not performed/inadequate

Cited by Laurie B Frazier

14 Apr 2009
21 CFR 820.100(b)

Documentation

Cited by Laurie B Frazier

Inspected site

ATAgilent Technologies, IncWinooski, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.50(a)(2)Cited across public-safe Form 483 observations1x
21 CFR 820.100(b)Cited across public-safe Form 483 observations1x
21 CFR 820.30(g)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 3 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