Form 483

Ease Seating Systems, Inc. Form 483, 2024-04-30

FDA issued a Form 483 to Ease Seating Systems, Inc. on 2024-04-30 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Ease Seating Systems, Inc. · Clio, United States · Issued April 30, 2024

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

30 Apr 2024
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Felicia E Hinojosa, Felicia E Armbrustmacher

30 Apr 2024
21 CFR 820.30(a)

Design control - no procedures

Cited by Felicia E Hinojosa, Felicia E Armbrustmacher

30 Apr 2024
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Felicia E Hinojosa, Felicia E Armbrustmacher

30 Apr 2024
21 CFR 830.310(b)

GUDID Information required for unique device identification.

Cited by Felicia E Hinojosa, Felicia E Armbrustmacher

Inspected site

ESEase Seating Systems, Inc.Clio, 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 observations1x
21 CFR 820.30(a)Cited across public-safe Form 483 observations1x
21 CFR 820.50Cited across public-safe Form 483 observations1x
21 CFR 830.310(b)Cited across public-safe Form 483 observations1x

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 4 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