Form 483

CORTRONIK GmbH Form 483, 2015-09-17

FDA issued a Form 483 to CORTRONIK GmbH on 2015-09-17 with 5 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health5 observations

CORTRONIK GmbH · Rostock, Germany · Issued September 17, 2015

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.

17 Sep 2015
21 CFR 820.100(b)

Documentation

Cited by Michelle J Glembin

17 Sep 2015
21 CFR 820.181

DMR - not or inadequately maintained

Cited by Michelle J Glembin

17 Sep 2015
21 CFR 820.30(c)

Design input - documentation

Cited by Michelle J Glembin

17 Sep 2015
21 CFR 820.75(a)

Documentation

Cited by Michelle J Glembin

17 Sep 2015
21 CFR 820.90(a)

Nonconforming product, Lack of or inadequate procedures

Cited by Michelle J Glembin

Inspected site

CGCORTRONIK GmbHRostock, Germany

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(b)Cited across public-safe Form 483 observations1x
21 CFR 820.181Cited across public-safe Form 483 observations1x
21 CFR 820.30(c)Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x
21 CFR 820.90(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 5 observations

The full inspection record, as Atlas holds it, 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