Form 483

SoClean, Inc Form 483, 2023-02-06

FDA issued a Form 483 to SoClean, Inc on 2023-02-06 with 10 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health10 observations

SoClean, Inc · Peterborough, United States · Issued February 6, 2023

Overview

  • 10 public-safe observations are available for this inspection.
  • 5 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.

6 Feb 2023
21 CFR 803.50(a)(2)

Individual Report of Malfunction

Cited by Stephen C Smith, Katarzyna Plona

6 Feb 2023
21 CFR 803.50(a)(2)

Individual Report of Malfunction

Cited by Stephen C Smith, Katarzyna Plona

6 Feb 2023
21 CFR 820.184

Lack of or inadequate DHR procedures

Cited by Stephen C Smith, Katarzyna Plona

6 Feb 2023
21 CFR 820.184

Lack of or inadequate DHR procedures

Cited by Stephen C Smith, Katarzyna Plona

6 Feb 2023
21 CFR 820.22

Quality Audit/Reaudit - conducted

Cited by Stephen C Smith, Katarzyna Plona

Inspected site

SISoClean, IncPeterborough, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.50(a)(2)Cited across public-safe Form 483 observations2x
21 CFR 820.184Cited across public-safe Form 483 observations2x
21 CFR 820.22Cited across public-safe Form 483 observations2x
21 CFR 820.86Cited across public-safe Form 483 observations2x
21 CFR 820.90(b)(1)Cited 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 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