Form 483

AMS Diagnostics, LLC Form 483, 2020-01-21

FDA issued a Form 483 to AMS Diagnostics, LLC on 2020-01-21 with 10 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health10 observations

AMS Diagnostics, LLC · Weston, United States · Issued January 21, 2020

Overview

  • 10 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 Jan 2020
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Dianiris C Ayala

21 Jan 2020
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Dianiris C Ayala

21 Jan 2020
21 CFR 820.20(b)

Lack of or inadequate organizational structure

Cited by Dianiris C Ayala

21 Jan 2020
21 CFR 820.20(b)

Lack of or inadequate organizational structure

Cited by Dianiris C Ayala

21 Jan 2020
21 CFR 820.20(b)(3)

Management representative

Cited by Dianiris C Ayala

Inspected site

ADAMS Diagnostics, LLCWeston, 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 observations2x
21 CFR 820.20(b)Cited across public-safe Form 483 observations2x
21 CFR 820.20(b)(3)Cited across public-safe Form 483 observations2x
21 CFR 820.20(c)Cited across public-safe Form 483 observations2x
21 CFR 820.22Cited 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 10 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