Form 483

Avid Medical, Inc. Form 483, 2022-12-05

FDA issued a Form 483 to Avid Medical, Inc. on 2022-12-05 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

Avid Medical, Inc. · Toano, United States · Issued December 5, 2022

Overview

  • 6 public-safe observations are available for this inspection.
  • 3 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.

5 Dec 2022
21 CFR 820.72(a)

Calibration, Inspection, etc. Procedures Lack of or Inadequ

Cited by Tiki Dixon

5 Dec 2022
21 CFR 820.72(a)

Calibration, Inspection, etc. Procedures Lack of or Inadequ

Cited by Tiki Dixon

5 Dec 2022
21 CFR 820.80(c)

Lack of or inadequate In-process acceptance procedures

Cited by Tiki Dixon

5 Dec 2022
21 CFR 820.80(c)

Lack of or inadequate In-process acceptance procedures

Cited by Tiki Dixon

5 Dec 2022
21 CFR 820.90(a)

Nonconforming product control

Cited by Tiki Dixon

Inspected site

AMAvid Medical, Inc.Toano, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.72(a)Cited across public-safe Form 483 observations2x
21 CFR 820.80(c)Cited across public-safe Form 483 observations2x
21 CFR 820.90(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 6 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