FDA-Inspected Site

Stericycle Inc

2 FDA inspections are on record for Stericycle Inc in Aurora, United States.

483· Form 483 issued

Aurora, United States · 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 2023-12-21.

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 Dec 2023 – 21 Dec 2023Medical Devices & Rad Health483View 483 →
7 Feb 2018 – 21 Feb 2018Medical Devices & Rad Health483View 483 →

Observations on record

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

21 Dec 2023
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Brittani N Franklin

21 Dec 2023
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Brittani N Franklin

21 Dec 2023
21 CFR 820.20(c)

Management review - defined interval, sufficient frequency

Cited by Brittani N Franklin

21 Dec 2023
21 CFR 820.20(c)

Management review - defined interval, sufficient frequency

Cited by Brittani N Franklin

21 Dec 2023
21 CFR 820.22

Quality audits - Lack of or inadequate procedures

Cited by Brittani N Franklin

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 820.20(c)Cited across public-safe Form 483 observations4x
21 CFR 820.22Cited across public-safe Form 483 observations4x
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x
21 CFR 820.198(a)Cited across public-safe Form 483 observations2x
21 CFR 820.50Cited across public-safe Form 483 observations2x
21 CFR 820.80(a)Cited across public-safe Form 483 observations2x

Full site report

Get the verbatim findings behind Stericycle Inc's 2 Form 483s

Source PDFs 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