FDA-Inspected Site

BIOTECH EUROPE MEDITECH Inc. Ltd

2 FDA inspections are on record for BIOTECH EUROPE MEDITECH Inc. Ltd in Roscommon, Ireland.

Clean· No action indicated

Roscommon, Ireland · Last updated July 11, 2026

Overview

  • 2 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2025-03-26.

At a glance

Inspections

2

Form 483s

1

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
24 Mar 2025 – 26 Mar 2025Medical Devices & Rad HealthClean
11 Apr 2022 – 14 Apr 2022Medical Devices & Rad Health483On file

Observations on record

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

14 Apr 2022
21 CFR 820.100(b)

Documentation

Cited by Esteban Beltran

14 Apr 2022
21 CFR 820.22

Quality audits - auditor independence

Cited by Esteban Beltran

14 Apr 2022
21 CFR 820.70(a)

Production processes

Cited by Esteban Beltran

14 Apr 2022
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by Esteban Beltran

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(b)Cited across public-safe Form 483 observations1x
21 CFR 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.70(a)Cited 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 BIOTECH EUROPE MEDITECH Inc. Ltd'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

Related sites