Form 483

Rafarm S.A. Form 483, 2017-10-17

FDA issued a Form 483 to Rafarm S.A. on 2017-10-17 with 5 public-safe observations.

483· Form 483 issuedHuman Drugs5 observations

Rafarm S.A. · Paiania, Greece · Issued October 17, 2017

Overview

  • 5 public-safe observations are available for this inspection.
  • 5 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.

17 Oct 2017
21 CFR 211.142(b)

Storage under appropriate conditions

Cited by Junho Pak

17 Oct 2017
21 CFR 211.160(b)

Scientifically sound laboratory controls

Cited by Junho Pak

17 Oct 2017
21 CFR 211.188(b)(13)

Results of drug product inspections and examinations

Cited by Junho Pak

17 Oct 2017
21 CFR 211.194(a)

Complete test data included in records

Cited by Junho Pak

17 Oct 2017
21 CFR 211.42(c)(10)(vi)

Equipment to control conditions

Cited by Junho Pak

Inspected site

RSRafarm S.A.Paiania, Greece

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.142(b)Cited across public-safe Form 483 observations1x
21 CFR 211.160(b)Cited across public-safe Form 483 observations1x
21 CFR 211.188(b)(13)Cited across public-safe Form 483 observations1x
21 CFR 211.194(a)Cited across public-safe Form 483 observations1x
21 CFR 211.42(c)(10)(vi)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 5 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