FDA-Inspected Site

UIH Technologies LLC

1 FDA inspection is on record for UIH Technologies LLC in Houston, United States.

483· Form 483 issued

Houston, United States · Last updated August 15, 2026

Overview

  • 1 FDA inspection is on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2025-08-20.

At a glance

Inspections

1

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
6 Aug 2025 – 20 Aug 2025Medical Devices & Rad Health483View 483 →

Observations on record

Form 483 observations cited at this site, most recent first.

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

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

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

Full site report

Get the verbatim findings behind UIH Technologies LLC's 1 Form 483

Source PDFs and recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat