Form 483

Catalent Pharma Solutions, LLC Form 483, 2018-06-14

FDA issued a Form 483 to Catalent Pharma Solutions, LLC on 2018-06-14 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

Catalent Pharma Solutions, LLC · Saint Petersburg, United States · Issued June 14, 2018

Overview

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

14 Jun 2018
21 CFR 211.110(a)

Written in-process control procedures

Cited by Jennifer Lalama, Christos G Tsingelis

14 Jun 2018
21 CFR 211.113(a)

Procedures for non-sterile drug products

Cited by Jennifer Lalama, Christos G Tsingelis

14 Jun 2018
21 CFR 211.192

Quality control unit review of records

Cited by Jennifer Lalama, Christos G Tsingelis

14 Jun 2018
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Jennifer Lalama, Christos G Tsingelis

Inspected site

CPCatalent Pharma Solutions, LLCSaint Petersburg, United States

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 211.113(a)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x

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 4 observations

The source PDF and 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