Form 483

Fluke Biomedical LLC Form 483, 2024-01-18

FDA issued a Form 483 to Fluke Biomedical LLC on 2024-01-18 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Fluke Biomedical LLC · Everett, United States · Issued January 18, 2024

Overview

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

18 Jan 2024
21 CFR 806.20(b)(4)

Justification for not reporting

Cited by Stephen R Souza, Brian R Hendricks

18 Jan 2024
21 CFR 806.20(b)(4)

Justification for not reporting

Cited by Stephen R Souza, Brian R Hendricks

18 Jan 2024
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Stephen R Souza, Brian R Hendricks

18 Jan 2024
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Stephen R Souza, Brian R Hendricks

Inspected site

FBFluke Biomedical LLCEverett, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 806.20(b)(4)Cited across public-safe Form 483 observations2x
21 CFR 820.100(a)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 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