FDA-Inspected Site

taberna pro medicum

2 FDA inspections are on record for taberna pro medicum in Luneburg, Germany.

483· Form 483 issued

Luneburg, 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 2018-06-14.

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
11 Jun 2018 – 14 Jun 2018Medical Devices & Rad Health483View 483 →
1 Nov 2012Not recorded483View 483 →

Observations on record

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

14 Jun 2018
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Amanda Dinaro

14 Jun 2018
21 CFR 820.198(b)

Review and evaluation for investigation

Cited by Amanda Dinaro

1 Nov 2012
21 CFR 820.22

Quality audits - auditor independence

Cited by Melissa I Michurski

1 Nov 2012
21 CFR 820.30(f)

Design verification - Lack of or inadequate procedures

Cited by Melissa I Michurski

1 Nov 2012
21 CFR 820.90(a)

Nonconforming product, Lack of or inadequate procedures

Cited by Melissa I Michurski

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 820.198(a)Cited across public-safe Form 483 observations2x
21 CFR 820.184Cited across public-safe Form 483 observations1x
21 CFR 820.198(b)Cited across public-safe Form 483 observations1x
21 CFR 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.30(f)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 taberna pro medicum's 2 Form 483s

Source PDFs, verbatim observations, 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