FDA-Inspected Site

Qiagen GmbH

8 FDA inspections are on record for Qiagen GmbH in Hilden, Germany.

Clean· No action indicated

Hilden, Germany · Last updated July 10, 2026

Overview

  • 8 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2026-03-12.

At a glance

Inspections

8

Form 483s

1

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
9 Mar 2026 – 12 Mar 2026Medical Devices & Rad HealthClean
31 Oct 2022 – 4 Nov 2022Medical Devices & Rad Health483On file
27 Jan 2020 – 30 Jan 2020Medical Devices & Rad HealthClean
6 Feb 2017 – 9 Feb 2017Medical Devices & Rad HealthClean
24 Aug 2015 – 27 Aug 2015Medical Devices & Rad HealthClean
4 Mar 2014 – 6 Mar 2014Medical Devices & Rad HealthClean
23 Sep 2013 – 26 Sep 2013Medical Devices & Rad HealthClean
24 Feb 2012Not recordedClean

Investigators

FDA investigators tied to this site in the record.

Full site report

Get the verbatim findings behind Qiagen GmbH's 1 Form 483

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