Form 483

Eriochem SA Form 483, 2018-05-22

FDA issued a Form 483 to Eriochem SA on 2018-05-22 with 5 public-safe observations.

483· Form 483 issuedHuman Drugs5 observations

Eriochem SA · Parana, Argentina · Issued May 22, 2018

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.

22 May 2018
21 CFR 211.113(b)

Validation lacking for sterile drug products

Cited by Santos E Camara

22 May 2018
21 CFR 211.42(c)

Defined areas of adequate size for operations

Cited by Santos E Camara

22 May 2018
21 CFR 211.42(c)(10)(vi)

Equipment to control conditions

Cited by Santos E Camara

22 May 2018
21 CFR 211.42(c)(10)(v)

Cleaning System

Cited by Santos E Camara

22 May 2018
21 CFR 211.58

Buildings not maintained in good state of repair

Cited by Santos E Camara

Inspected site

ESEriochem SAParana, Argentina

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 211.42(c)Cited across public-safe Form 483 observations1x
21 CFR 211.42(c)(10)(v)Cited across public-safe Form 483 observations1x
21 CFR 211.42(c)(10)(vi)Cited across public-safe Form 483 observations1x
21 CFR 211.58Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 5 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