Form 483

Acorn Stairlifts, Inc Form 483, 2018-09-04

FDA issued a Form 483 to Acorn Stairlifts, Inc on 2018-09-04 with 10 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health10 observations

Acorn Stairlifts, Inc · Belle Isle, United States · Issued September 4, 2018

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.

4 Sep 2018
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Richard K Vogel

4 Sep 2018
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Richard K Vogel

4 Sep 2018
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Richard K Vogel

4 Sep 2018
21 CFR 803.50(a)(1)

Report of Death or Serious Injury

Cited by Richard K Vogel

4 Sep 2018
21 CFR 803.50(a)(1)

Report of Death or Serious Injury

Cited by Richard K Vogel

Inspected site

ASAcorn Stairlifts, IncBelle Isle, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.50(a)(1)Cited across public-safe Form 483 observations2x
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x
21 CFR 820.22Cited across public-safe Form 483 observations2x
21 CFR 820.30(i)Cited across public-safe Form 483 observations2x
21 CFR 820.50Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 10 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