Form 483

DRG Instruments GmbH Form 483, 2010-10-21

FDA issued a Form 483 to DRG Instruments GmbH on 2010-10-21 with 3 public-safe observations.

483· Form 483 issued3 observations

DRG Instruments GmbH · Marburg, Germany · Issued October 21, 2010

Overview

  • 3 public-safe observations are available for this inspection.
  • 3 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.

21 Oct 2010
21 CFR 820.80(e)

Documentation

Cited by Rodney D Combs

21 Oct 2010
21 CFR 820.90(b)(2)

Product rework documentation, DHR {see also 820.184}

Cited by Rodney D Combs

21 Oct 2010
21 CFR 820.181

DMR - not or inadequately maintained

Cited by Rodney D Combs

Inspected site

DIDRG Instruments GmbHMarburg, Germany

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.181Cited across public-safe Form 483 observations1x
21 CFR 820.80(e)Cited across public-safe Form 483 observations1x
21 CFR 820.90(b)(2)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 3 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