Form 483

Myriad Medical, LLC Form 483, 2019-10-17

FDA issued a Form 483 to Myriad Medical, LLC on 2019-10-17 with 20 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health20 observations

Myriad Medical, LLC · Tampa, United States · Issued October 17, 2019

Overview

  • 20 public-safe observations are available for this inspection.
  • 7 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.

17 Oct 2019
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Joshua J Silvestri

17 Oct 2019
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Joshua J Silvestri

17 Oct 2019
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Joshua J Silvestri

17 Oct 2019
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Joshua J Silvestri

17 Oct 2019
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Joshua J Silvestri

Inspected site

MMMyriad Medical, LLCTampa, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.198(a)Cited across public-safe Form 483 observations4x
21 CFR 820.22Cited across public-safe Form 483 observations4x
21 CFR 820.50(a)(3)Cited across public-safe Form 483 observations4x
21 CFR 803.17Cited across public-safe Form 483 observations2x
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x
21 CFR 820.30(j)Cited across public-safe Form 483 observations2x
21 CFR 820.50Cited across public-safe Form 483 observations2x

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 20 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