Form 483

Merz Pharma GmbH & Co KGaA Form 483, 2019-11-22

FDA issued a Form 483 to Merz Pharma GmbH & Co KGaA on 2019-11-22 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

Merz Pharma GmbH & Co KGaA · Dessau-Rosslau, Germany · Issued November 22, 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.

22 Nov 2019
21 CFR 211.100(b)

SOPs not followed / documented

Cited by Yumi J Hiramine, Susan T Hadman

22 Nov 2019
21 CFR 211.160(b)

Scientifically sound laboratory controls

Cited by Yumi J Hiramine, Susan T Hadman

22 Nov 2019
21 CFR 211.165(e)

Test methods

Cited by Yumi J Hiramine, Susan T Hadman

22 Nov 2019
21 CFR 600.14(a)(1)

Who must report - manufacturer

Cited by Yumi J Hiramine, Susan T Hadman

Inspected site

MPMerz Pharma GmbH & Co KGaADessau-Rosslau, Germany

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.100(b)Cited across public-safe Form 483 observations1x
21 CFR 211.160(b)Cited across public-safe Form 483 observations1x
21 CFR 211.165(e)Cited across public-safe Form 483 observations1x
21 CFR 600.14(a)(1)Cited across public-safe Form 483 observations1x

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, 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