Form 483

Fareva Amboise Form 483, 2011-09-20

FDA issued a Form 483 to Fareva Amboise on 2011-09-20 with 4 public-safe observations.

483· Form 483 issued4 observations

Fareva Amboise · Poce Sur Cisse, France · Issued September 20, 2011

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 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.

20 Sep 2011
21 CFR 211.110(a)

Control procedures to monitor and validate performance

Cited by Russell J Glapion

20 Sep 2011
21 CFR 211.110(b)

In-process materials specifications

Cited by Russell J Glapion

20 Sep 2011
21 CFR 211.165(f)

Failing drug products not rejected

Cited by Russell J Glapion

20 Sep 2011
21 CFR 211.192

Extent of discrepancy, failure investigations

Cited by Russell J Glapion

Inspected site

FAFareva AmboisePoce Sur Cisse, France

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.110(a)Cited across public-safe Form 483 observations1x
21 CFR 211.110(b)Cited across public-safe Form 483 observations1x
21 CFR 211.165(f)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 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