Form 483

Solupharm Pharmazeutische Erzeugnisse Gmbh Form 483, 2014-09-22

FDA issued a Form 483 to Solupharm Pharmazeutische Erzeugnisse Gmbh on 2014-09-22 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

Solupharm Pharmazeutische Erzeugnisse Gmbh · Melsungen, Germany · Issued September 22, 2014

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.

22 Sep 2014
21 CFR 211.42(c)(10)(iv)

Environmental Monitoring System

Cited by Carla A Norris, Karen E Dorazio

22 Sep 2014
21 CFR 211.111

Deviations of production time limits

Cited by Carla A Norris, Karen E Dorazio

22 Sep 2014
21 CFR 211.160(b)

Scientifically sound laboratory controls

Cited by Carla A Norris, Karen E Dorazio

22 Sep 2014
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Carla A Norris, Karen E Dorazio

Inspected site

Inspection team

KEKaren E Dorazio

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.111Cited across public-safe Form 483 observations1x
21 CFR 211.160(b)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.42(c)(10)(iv)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 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