Form 483

UIH Technologies LLC Form 483, 2025-08-20

FDA issued a Form 483 to UIH Technologies LLC on 2025-08-20 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

UIH Technologies LLC · Houston, United States · Issued August 20, 2025

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.

20 Aug 2025
21 CFR 801.40(a)

Form of a unique device identifier

Cited by Ellen J Tave

20 Aug 2025
21 CFR 801.40(a)

Form of a unique device identifier

Cited by Ellen J Tave

20 Aug 2025
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Ellen J Tave

20 Aug 2025
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Ellen J Tave

20 Aug 2025
21 CFR 820.80(d)

Lack of or inadequate final acceptance procedures

Cited by Ellen J Tave

Inspected site

UTUIH Technologies LLCHouston, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 801.40(a)Cited across public-safe Form 483 observations2x
21 CFR 820.198(a)Cited across public-safe Form 483 observations2x
21 CFR 820.80(d)Cited across public-safe Form 483 observations2x

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 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