FDA-Inspected Site

Pausch Medical GmbH

3 FDA inspections are on record for Pausch Medical GmbH in Erlangen, Germany.

483· Form 483 issued

Erlangen, Germany · Last updated August 15, 2026

Overview

  • 3 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2026-04-01.

At a glance

Inspections

3

Form 483s

2

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
30 Mar 2026 – 1 Apr 2026Medical Devices & Rad Health483View 483 →
21 Feb 2023 – 24 Feb 2023Medical Devices & Rad Health483View 483 →
13 Aug 2018 – 15 Aug 2018Medical Devices & Rad HealthClean

Observations on record

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

1 Apr 2026
21 CFR 1002.10

Failure to submit, distinct marking

Cited by Benjamin W Anderson

24 Feb 2023
21 CFR 1002.10

Failure to submit, distinct marking

Cited by Eric C Schmitt

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 1002.10Cited across public-safe Form 483 observations2x

Full site report

Get the verbatim findings behind Pausch Medical GmbH's 2 Form 483s

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