Form 483

Tutogen Medical GmbH Form 483, 2017-01-26

FDA issued a Form 483 to Tutogen Medical GmbH on 2017-01-26 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Tutogen Medical GmbH · Neunkirchen A. Brand, Germany · Issued January 26, 2017

Overview

  • 4 public-safe observations are available for this inspection.
  • 2 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.

26 Jan 2017
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Frank J Marciniak

26 Jan 2017
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Frank J Marciniak

26 Jan 2017
21 CFR 820.70(c)

Environmental control Lack of or inadequate procedures

Cited by Frank J Marciniak

26 Jan 2017
21 CFR 820.70(c)

Environmental control Lack of or inadequate procedures

Cited by Frank J Marciniak

Inspected site

TMTutogen Medical GmbHNeunkirchen A. Brand, Germany

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x
21 CFR 820.70(c)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 4 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