Form 483

Catalent Pharma Solutions, LLC Form 483, 2019-08-28

FDA issued a Form 483 to Catalent Pharma Solutions, LLC on 2019-08-28 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Catalent Pharma Solutions, LLC · Saint Petersburg, United States · Issued August 28, 2019

Overview

  • 4 public-safe observations are available for this inspection.
  • 2 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.

28 Aug 2019
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by Joshua J Silvestri

28 Aug 2019
21 CFR 820.90(a)

Nonconforming product, Lack of or inadequate procedures

Cited by Joshua J Silvestri

28 Aug 2019
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by Joshua J Silvestri

28 Aug 2019
21 CFR 820.90(a)

Nonconforming product, Lack of or inadequate procedures

Cited by Joshua J Silvestri

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 820.75(a)Cited across public-safe Form 483 observations2x
21 CFR 820.90(a)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 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