Form 483

CorePharma, LLC Form 483, 2008-11-14

FDA issued a Form 483 to CorePharma, LLC on 2008-11-14 with 8 public-safe observations.

483· Form 483 issued8 observations

CorePharma, LLC · Middlesex, United States · Issued November 14, 2008

Overview

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

14 Nov 2008
21 CFR 211.80(a)

Written Procedures Not Followed

Cited by Kristy A Zielny

14 Nov 2008
21 CFR 211.100(a)

Changes to Procedures Not Reviewed, Approved

Cited by Kristy A Zielny

14 Nov 2008
21 CFR 211.100(b)

Procedure Deviations Recorded and Justified

Cited by Kristy A Zielny

14 Nov 2008
21 CFR 211.192

Extent of discrepancy, failure investigations

Cited by Kristy A Zielny

14 Nov 2008
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Kristy A Zielny

Inspected site

CLCorePharma, LLCMiddlesex, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.192Cited across public-safe Form 483 observations3x
21 CFR 211.100(a)Cited across public-safe Form 483 observations1x
21 CFR 211.100(b)Cited across public-safe Form 483 observations1x
21 CFR 211.198(a)Cited across public-safe Form 483 observations1x
21 CFR 211.80(a)Cited across public-safe Form 483 observations1x
21 CFR 314.80(c)(2)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 8 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