Form 483

AADCO Medical Inc. Form 483, 2023-02-22

FDA issued a Form 483 to AADCO Medical Inc. on 2023-02-22 with 5 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health5 observations

AADCO Medical Inc. · Randolph, United States · Issued February 22, 2023

Overview

  • 5 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.

22 Feb 2023
21 CFR 820.184

Lack of or inadequate DHR procedures

Cited by Stephen C Smith

22 Feb 2023
21 CFR 820.30(e)

Design review - Lack of or inadequate procedures

Cited by Stephen C Smith

22 Feb 2023
21 CFR 820.30(j)

Design history file

Cited by Stephen C Smith

22 Feb 2023
21 CFR 820.75(b)(2)

Documentation of validated process performance

Cited by Stephen C Smith

22 Feb 2023
21 CFR 820.86

Acceptance status

Cited by Stephen C Smith

Inspected site

AMAADCO Medical Inc.Randolph, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.184Cited across public-safe Form 483 observations1x
21 CFR 820.30(e)Cited across public-safe Form 483 observations1x
21 CFR 820.30(j)Cited across public-safe Form 483 observations1x
21 CFR 820.75(b)(2)Cited across public-safe Form 483 observations1x
21 CFR 820.86Cited across public-safe Form 483 observations1x

Source document

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PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 5 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