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Form 483

Philips Respironics, Inc. Form 483, 2014-04-15

FDA issued a Form 483 to Philips Respironics, Inc. on 2014-04-15 with 2 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health2 observations

Philips Respironics, Inc. · Murrysville, United States · Issued April 15, 2014

Overview

  • 2 public-safe observations are available for this inspection.
  • 2 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.

15 Apr 2014
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Katelyn A Staub-Zamperini

15 Apr 2014
21 CFR 820.70(a)

Production processes

Cited by Katelyn A Staub-Zamperini

Inspected site

PRPhilips Respironics, Inc.Murrysville, United States

Inspection team

KAKatelyn A Staub-Zamperini

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.50Cited across public-safe Form 483 observations1x
21 CFR 820.70(a)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.

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Full 483 report

Get the verbatim text of all 2 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