Form 483

W. Kroemker GmbH Form 483, 2018-04-06

FDA issued a Form 483 to W. Kroemker GmbH on 2018-04-06 with 5 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health5 observations

W. Kroemker GmbH · Buckeburg, Germany · Issued April 6, 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.

6 Apr 2018
21 CFR 820.181

DMR - not or inadequately maintained

Cited by Claudette D Brooks

6 Apr 2018
21 CFR 820.20(b)

Lack of or inadequate organizational structure

Cited by Claudette D Brooks

6 Apr 2018
21 CFR 820.30(e)

Design review - documentation

Cited by Claudette D Brooks

6 Apr 2018
21 CFR 820.200(a)

Servicing - Lack of or inadequate procedures

Cited by Claudette D Brooks

6 Apr 2018
21 CFR 820.80(b)

Lack of or inadequate receiving acceptance procedures

Cited by Claudette D Brooks

Inspected site

WKW. Kroemker GmbHBuckeburg, 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 820.20(b)Cited across public-safe Form 483 observations1x
21 CFR 820.200(a)Cited across public-safe Form 483 observations1x
21 CFR 820.30(e)Cited across public-safe Form 483 observations1x
21 CFR 820.80(b)Cited 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