FDA-Inspected Site

Steris Corporation

6 FDA inspections are on record for Steris Corporation in Saint Louis, United States.

483· Form 483 issued

Saint Louis, United States · Last updated July 10, 2026

Overview

  • 6 FDA inspections are on record.
  • 3 inspections produced a Form 483.
  • The most recent recorded inspection date is 2023-11-06.

At a glance

Inspections

6

Form 483s

3

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
1 Nov 2023 – 6 Nov 2023Human Drugs483On file
6 Jun 2016 – 8 Jun 2016Medical Devices & Rad HealthClean
23 Feb 2015 – 27 Feb 2015Medical Devices & Rad Health483View 483 →
17 May 2011Not recordedClean
16 Jul 2009Not recorded483On file
3 May 2001Not recordedClean

Observations on record

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

27 Feb 2015
21 CFR 211.100(a)

Absence of Written Procedures

Cited by Eric M Padgett, Edward E Lockwood

27 Feb 2015
21 CFR 211.58

Buildings not maintained in good state of repair

Cited by Eric M Padgett, Edward E Lockwood

27 Feb 2015
21 CFR 211.65(b)

Substances That Come in Contact

Cited by Eric M Padgett, Edward E Lockwood

Investigators

FDA investigators tied to this site in the record.

Adree N Anderson2 insp.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 211.100(a)Cited across public-safe Form 483 observations1x
21 CFR 211.58Cited across public-safe Form 483 observations1x
21 CFR 211.65(b)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Steris Corporation's 3 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