Form 483

Chiesi Farmaceutici S.p.A. Form 483, 2019-05-24

FDA issued a Form 483 to Chiesi Farmaceutici S.p.A. on 2019-05-24 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

Chiesi Farmaceutici S.p.A. · Parma, Italy · Issued May 24, 2019

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.

24 May 2019
21 CFR 211.113(b)

Validation lacking for sterile drug products

Cited by Saleem A Akhtar, Scott R Nichols

24 May 2019
21 CFR 211.160(b)(3)

Acceptance of drug products

Cited by Saleem A Akhtar, Scott R Nichols

24 May 2019
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Saleem A Akhtar, Scott R Nichols

24 May 2019
21 CFR 211.56(a)

Sanitation--buildings not clean, free of infestation

Cited by Saleem A Akhtar, Scott R Nichols

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.113(b)Cited across public-safe Form 483 observations1x
21 CFR 211.160(b)(3)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.56(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 observations

The full inspection record, as Atlas holds it, 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