Form 483

Centurion Medical Products Corporation Form 483, 2019-08-20

FDA issued a Form 483 to Centurion Medical Products Corporation on 2019-08-20 with 18 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health18 observations

Centurion Medical Products Corporation · Howell, United States · Issued August 20, 2019

Overview

  • 18 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.

20 Aug 2019
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Thomas A Peter

20 Aug 2019
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Thomas A Peter

20 Aug 2019
21 CFR 820.70(c)

Environmental control Lack of or inadequate procedures

Cited by Thomas A Peter

20 Aug 2019
21 CFR 820.70(c)

Environmental control Lack of or inadequate procedures

Cited by Thomas A Peter

20 Aug 2019
21 CFR 820.70(i)

Software validation for automated processes

Cited by Thomas A Peter

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.70(c)Cited across public-safe Form 483 observations6x
21 CFR 820.75(a)Cited across public-safe Form 483 observations6x
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x
21 CFR 820.70(i)Cited across public-safe Form 483 observations2x
21 CFR 820.80(a)Cited across public-safe Form 483 observations2x

Source document

PDF
PDF available

Form 483 source document

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Full 483 report

Get the verbatim text of all 18 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