Form 483

Tiadent Inc Form 483, 2026-02-11

FDA issued a Form 483 to Tiadent Inc on 2026-02-11 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

Tiadent Inc · Rosenberg, United States · Issued February 11, 2026

Overview

  • 3 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.

11 Feb 2026
21 CFR 801.20(a)

Label to bear a unique device identifier

Cited by Jocelyn C Turner

11 Feb 2026
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Jocelyn C Turner

11 Feb 2026
ISO 13485:2016 Clause 4.1.2

Risk-based approach not applied to QMS processes

Cited by Jocelyn C Turner

Inspected site

TITiadent IncRosenberg, 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 observations1x
21 CFR 803.17Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 4.1.2Cited across public-safe Form 483 observations1x

Source document

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Form 483 source document

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Full 483 report

Get the verbatim text of all 3 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