Form 483

Stericycle Inc Form 483, 2018-02-21

FDA issued a Form 483 to Stericycle Inc on 2018-02-21 with 10 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health10 observations

Stericycle Inc · Aurora, United States · Issued February 21, 2018

Overview

  • 10 public-safe observations are available for this inspection.
  • 5 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

21 Feb 2018
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Amanda Dinaro

21 Feb 2018
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Amanda Dinaro

21 Feb 2018
21 CFR 820.20(c)

Management review - Lack of or inadequate procedures

Cited by Amanda Dinaro

21 Feb 2018
21 CFR 820.20(c)

Management review - Lack of or inadequate procedures

Cited by Amanda Dinaro

21 Feb 2018
21 CFR 820.22

Quality Audit/Reaudit - conducted

Cited by Amanda Dinaro

Inspected site

SIStericycle IncAurora, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.198(a)Cited across public-safe Form 483 observations2x
21 CFR 820.20(c)Cited across public-safe Form 483 observations2x
21 CFR 820.22Cited 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 483 report

Get the verbatim text of all 10 observations

The full inspection record, as Atlas holds it, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere