Form 483

Penner Patient Care, Inc. Form 483, 2025-02-11

FDA issued a Form 483 to Penner Patient Care, Inc. on 2025-02-11 with 8 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health8 observations

Penner Patient Care, Inc. · Aurora, United States · Issued February 11, 2025

Overview

  • 8 public-safe observations are available for this inspection.
  • 4 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.

11 Feb 2025
21 CFR 801.20(a)

Label to bear a unique device identifier

Cited by Eric C Fox

11 Feb 2025
21 CFR 801.20(a)

Label to bear a unique device identifier

Cited by Eric C Fox

11 Feb 2025
21 CFR 803.17(a)(3)

Lack of System for Timely Submission of Reports

Cited by Eric C Fox

11 Feb 2025
21 CFR 803.17(a)(3)

Lack of System for Timely Submission of Reports

Cited by Eric C Fox

11 Feb 2025
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Eric C Fox

Inspected site

PPPenner Patient Care, Inc.Aurora, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 801.20(a)Cited across public-safe Form 483 observations2x
21 CFR 803.17(a)(3)Cited across public-safe Form 483 observations2x
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x
21 CFR 820.50(a)Cited across public-safe Form 483 observations2x

Source document

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Form 483 source document

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Full 483 report

Get the verbatim text of all 8 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