Form 483

Charles River Laboratories Form 483, 2016-04-15

FDA issued a Form 483 to Charles River Laboratories on 2016-04-15 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

Charles River Laboratories · Mattawan, United States · Issued April 15, 2016

Overview

  • 6 public-safe observations are available for this inspection.
  • 3 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.

15 Apr 2016
21 CFR 58.185(a)(10)

Final report: names of those involved

Cited by Byron Ho

15 Apr 2016
21 CFR 58.33(f)

Study director: transfer of data to archives

Cited by Byron Ho

15 Apr 2016
21 CFR 58.35(b)(6)

QAU: review final study report

Cited by Byron Ho

15 Apr 2016
21 CFR 58.185(a)(10)

Final report: names of those involved

Cited by Byron Ho

15 Apr 2016
21 CFR 58.33(f)

Study director: transfer of data to archives

Cited by Byron Ho

Inspected site

CRCharles River LaboratoriesMattawan, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 58.185(a)(10)Cited across public-safe Form 483 observations2x
21 CFR 58.33(f)Cited across public-safe Form 483 observations2x
21 CFR 58.35(b)(6)Cited across public-safe Form 483 observations2x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 6 observations

The source PDF, 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