Form 483

Philips Visicu Form 483, 2016-04-19

FDA issued a Form 483 to Philips Visicu on 2016-04-19 with 14 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health14 observations

Philips Visicu · Baltimore, United States · Issued April 19, 2016

Overview

  • 14 public-safe observations are available for this inspection.
  • 6 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 2016
21 CFR 803.50(a)(2)

Report of Malfunction

Cited by Marc S Neubauer

19 Apr 2016
21 CFR 803.50(a)(2)

Report of Malfunction

Cited by Marc S Neubauer

19 Apr 2016
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Marc S Neubauer

19 Apr 2016
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Marc S Neubauer

19 Apr 2016
21 CFR 820.198(c)

Investigation of device failures

Cited by Marc S Neubauer

Inspected site

PVPhilips VisicuBaltimore, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.30(g)Cited across public-safe Form 483 observations4x
21 CFR 803.50(a)(2)Cited across public-safe Form 483 observations2x
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x
21 CFR 820.198(c)Cited across public-safe Form 483 observations2x
21 CFR 820.30(c)Cited across public-safe Form 483 observations2x
21 CFR 820.30(f)Cited across public-safe Form 483 observations2x

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 14 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