Form 483

Chartwell Pharmaceuticals West Caldwell, LLC. Form 483, 2016-05-25

FDA issued a Form 483 to Chartwell Pharmaceuticals West Caldwell, LLC. on 2016-05-25 with 3 public-safe observations.

483· Form 483 issuedHuman Drugs3 observations

Chartwell Pharmaceuticals West Caldwell, LLC. · West Caldwell, United States · Issued May 25, 2016

Overview

  • 3 public-safe observations are available for this inspection.
  • 3 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

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

25 May 2016
21 CFR 314.80(c)(2)(ii)(A)

Incomplete periodic safety report

Cited by Yvesna C Blaise, Jose M Cayuela

25 May 2016
21 CFR 314.80(b)

Failure to develop written procedures

Cited by Yvesna C Blaise, Jose M Cayuela

25 May 2016
21 CFR 314.80(c)(1)(i)

Late submission of 15-day report

Cited by Yvesna C Blaise, Jose M Cayuela

Inspected site

CPChartwell Pharmaceuticals West Caldwell, LLC.West Caldwell, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 314.80(b)Cited across public-safe Form 483 observations1x
21 CFR 314.80(c)(1)(i)Cited across public-safe Form 483 observations1x
21 CFR 314.80(c)(2)(ii)(A)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 3 observations

Every observation in full, 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