FDA-Inspected Site

Steris S.p.A.

5 FDA inspections are on record for Steris S.p.A. in Seriate, Italy.

483· Form 483 issued

Seriate, Italy · Last updated August 15, 2026

Overview

  • 5 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2026-02-26.

At a glance

Inspections

5

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
23 Feb 2026 – 26 Feb 2026Medical Devices & Rad Health483View 483 →
9 Sep 2013 – 12 Sep 2013Medical Devices & Rad HealthClean
19 Jan 2006Not recordedClean
6 Feb 2003Not recordedClean
8 Jun 2000Not recordedClean

Observations on record

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

26 Feb 2026
ISO 13485:2016 Clause 4.1.2

Risk-based approach not applied to QMS processes

Cited by Scott D Stevens

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
ISO 13485:2016 Clause 4.1.2Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Steris S.p.A.'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