FDA-Inspected Site

PFM Medical Mepro GMBH

3 FDA inspections are on record for PFM Medical Mepro GMBH in Nonnweiler, Germany.

483· Form 483 issued

Nonnweiler, Germany · Last updated July 10, 2026

Overview

  • 3 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2023-01-26.

At a glance

Inspections

3

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
23 Jan 2023 – 26 Jan 2023Medical Devices & Rad Health483View 483 →
27 Aug 2018 – 30 Aug 2018Medical Devices & Rad HealthClean
4 Feb 2013 – 7 Feb 2013Medical Devices & Rad HealthClean

Observations on record

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

26 Jan 2023
21 CFR 803.17(b)(4)

Info which facilitates timely FDA follow-up

Cited by Joshua J Silvestri

26 Jan 2023
21 CFR 820.90(a)

Nonconforming product, Lack of or inadequate procedures

Cited by Joshua J Silvestri

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 803.17(b)(4)Cited across public-safe Form 483 observations1x
21 CFR 820.90(a)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind PFM Medical Mepro GMBH's 1 Form 483

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