FDA-Inspected Site

Intertek USA Inc.

7 FDA inspections are on record for Intertek USA Inc. in Whitehouse, United States.

Clean· No action indicated

Whitehouse, United States · Last updated August 15, 2026

Overview

  • 7 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2025-09-25.

At a glance

Inspections

7

Form 483s

1

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
19 Sep 2025 – 25 Sep 2025Human DrugsClean
3 Mar 2025 – 7 Mar 2025Biologics483View 483 →
6 Nov 2020 – 21 Dec 2020Human DrugsClean
9 Aug 2016 – 12 Aug 2016Human DrugsClean
21 Jan 2013Not recordedClean
3 Mar 2010Not recordedClean
25 Jul 2001Not recordedClean

Observations on record

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

7 Mar 2025
21 CFR 11

Electronic records

Cited by Christian Lynch, Lizaida Perez

7 Mar 2025
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Christian Lynch, Lizaida Perez

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 11Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Intertek USA Inc.'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