FDA-Inspected Site

Procon Medizintechnik GmbH

2 FDA inspections are on record for Procon Medizintechnik GmbH in Alzenau, Germany.

483· Form 483 issued

Alzenau, Germany · Last updated July 10, 2026

Overview

  • 2 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2018-09-21.

At a glance

Inspections

2

Form 483s

2

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
19 Sep 2018 – 21 Sep 2018Medical Devices & Rad Health483View 483 →
6 Apr 2011Not recorded483On file

Observations on record

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

21 Sep 2018
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by James M Simpson

21 Sep 2018
21 CFR 820.250(b)

Sampling methods - Lack of or inadequate procedures

Cited by James M Simpson

21 Sep 2018
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by James M Simpson

21 Sep 2018
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by James M Simpson

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 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.250(b)Cited across public-safe Form 483 observations1x
21 CFR 820.50Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Procon Medizintechnik GmbH's 2 Form 483s

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