Tiadent Inc

FDA inspection history in Rosenberg, Texas, 2026

1
Form 483

Every document, by year

  • Form 483

2026: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2026One Form 483, at Rosenberg, Texas.

Cited most

Across all Tiadent observations on file

  • 21 CFR 803
    1
  • 21 CFR 830
    1
  • ISO 13485:2016 Clause 4.1.2
    What is the scope of this subpart?
    1
  • 21 CFR 801.20(a)
    Label to bear a unique device identifier
    1
  • 21 CFR 803.17
    What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?
    1

The complete Tiadent file.

All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.

$99

The documents one by one, while the file is prepared

See the documents

Sites

Documents

1 on file, newest first
DateDocumentPrice
2026-02-11483 Form 483$99

Investigators on these documents

Jocelyn C. Turner (1)

FEI number 3036042026 · most recent document Feb 11, 2026

About Tiadent Inc

How many FDA Form 483s has Tiadent Inc received?

FDA Intel has 1 Form 483 on file for Tiadent Inc; the most recent is dated Feb 11, 2026.

When was Tiadent Inc last inspected by FDA?

The most recent FDA inspection document on file for Tiadent Inc is a Form 483 dated Feb 11, 2026, for the site in Rosenberg, Texas.

What did FDA cite at Tiadent Inc?

The regulations cited most in the observations on file for Tiadent Inc are 21 CFR 803, 1 time; 21 CFR 830, 1 time; ISO 13485:2016 Clause 4.1.2 (What is the scope of this subpart?), 1 time.