Form 483

Magellan Diagnostics, Inc. Form 483, 2019-10-21

FDA issued a Form 483 to Magellan Diagnostics, Inc. on 2019-10-21 with 22 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health22 observations

Magellan Diagnostics, Inc. · North Billerica, United States · Issued October 21, 2019

Overview

  • 22 public-safe observations are available for this inspection.
  • 5 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.

21 Oct 2019
21 CFR 803.50(a)(2)

Individual Report of Malfunction

Cited by Sara M Onyango

21 Oct 2019
21 CFR 803.50(a)(2)

Individual Report of Malfunction

Cited by Sara M Onyango

21 Oct 2019
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Sara M Onyango

21 Oct 2019
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Sara M Onyango

21 Oct 2019
21 CFR 820.181

DMR - not or inadequately maintained

Cited by Sara M Onyango

Inspected site

MDMagellan Diagnostics, Inc.North Billerica, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.181Cited across public-safe Form 483 observations6x
21 CFR 820.198(a)Cited across public-safe Form 483 observations6x
21 CFR 820.30(g)Cited across public-safe Form 483 observations6x
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

Source document

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Form 483 source document

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Full 483 report

Get the verbatim text of all 22 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