Form 483

Otto Bock Healthcare Products GmbH Form 483, 2017-06-08

FDA issued a Form 483 to Otto Bock Healthcare Products GmbH on 2017-06-08 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Otto Bock Healthcare Products GmbH · Vienna, Austria · Issued June 8, 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.

8 Jun 2017
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Catherine J Laufmann

8 Jun 2017
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Catherine J Laufmann

8 Jun 2017
21 CFR 820.22

Quality audits - Lack of or inadequate procedures

Cited by Catherine J Laufmann

8 Jun 2017
21 CFR 820.22

Quality audits - Lack of or inadequate procedures

Cited by Catherine J Laufmann

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.198(a)Cited across public-safe Form 483 observations2x
21 CFR 820.22Cited 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