FDA-Inspected Site

Merz North America, Inc.

10 FDA inspections are on record for Merz North America, Inc. in Raleigh, United States.

Clean· No action indicated

Raleigh, United States · Last updated August 15, 2026

Overview

  • 10 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2025-10-28.

At a glance

Inspections

10

Form 483s

2

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
22 Oct 2025 – 28 Oct 2025Medical Devices & Rad HealthClean
20 Jun 2023 – 22 Jun 2023Medical Devices & Rad HealthClean
16 Sep 2019 – 18 Sep 2019Human DrugsClean
22 Jun 2017 – 23 Jun 2017Medical Devices & Rad HealthClean
4 Aug 2015 – 7 Aug 2015Human DrugsClean
26 Jan 2015Human DrugsClean
21 Jul 2011Not recorded483On file
29 Sep 2010Not recordedClean
15 Jan 2010Not recordedClean
24 Nov 2009Not recorded483On file

Investigators

FDA investigators tied to this site in the record.

Paul W Moy2 insp.
MDSAP WilliamsA1 insp.
Metitia G Sanders1 insp.
Jawaid Hamid1 insp.

Full site report

Get the verbatim findings behind Merz North America, Inc.'s 2 Form 483s

The full inspection record, as Atlas holds it, 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