Form 483

ABL Medical, LLC Form 483, 2015-05-21

FDA issued a Form 483 to ABL Medical, LLC on 2015-05-21 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

ABL Medical, LLC · American Fork, United States · Issued May 21, 2015

Overview

  • 4 public-safe observations are available for this inspection.
  • 2 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 May 2015
21 CFR 820.30(f)

Design verification - Lack of or inadequate procedures

Cited by Thai T Duong

21 May 2015
21 CFR 820.30(g)

Design validation- Lack of or inadequate procedures

Cited by Thai T Duong

21 May 2015
21 CFR 820.30(f)

Design verification - Lack of or inadequate procedures

Cited by Thai T Duong

21 May 2015
21 CFR 820.30(g)

Design validation- Lack of or inadequate procedures

Cited by Thai T Duong

Inspected site

AMABL Medical, LLCAmerican Fork, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.30(f)Cited across public-safe Form 483 observations2x
21 CFR 820.30(g)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 4 observations

Every observation in full, 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