Form 483

DeVilbiss Healthcare LLC Form 483, 2022-08-17

FDA issued a Form 483 to DeVilbiss Healthcare LLC on 2022-08-17 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

DeVilbiss Healthcare LLC · Somerset, United States · Issued August 17, 2022

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

17 Aug 2022
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Dennis R Hock, Lindsey L Kirsh

17 Aug 2022
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Dennis R Hock, Lindsey L Kirsh

17 Aug 2022
21 CFR 820.198(c)

Investigation of device failures

Cited by Dennis R Hock, Lindsey L Kirsh

17 Aug 2022
21 CFR 820.30(f)

Design verification - output does not meet input requirement

Cited by Dennis R Hock, Lindsey L Kirsh

Inspected site

DHDeVilbiss Healthcare LLCSomerset, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.198(c)Cited across public-safe Form 483 observations1x
21 CFR 820.30(f)Cited across public-safe Form 483 observations1x

Source document

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PDF available

Form 483 source document

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Full 483 report

Get the verbatim text of all 4 observations

The source PDF, 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