Form 483

Otto Bock Healthcare Products GmbH Form 483, 2019-11-21

FDA issued a Form 483 to Otto Bock Healthcare Products GmbH on 2019-11-21 with 8 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health8 observations

Otto Bock Healthcare Products GmbH · Vienna, Austria · Issued November 21, 2019

Overview

  • 8 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.

21 Nov 2019
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by John A Sciacchitano

21 Nov 2019
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by John A Sciacchitano

21 Nov 2019
21 CFR 820.70(i)

Software validation for automated processes

Cited by John A Sciacchitano

21 Nov 2019
21 CFR 820.70(i)

Software validation for automated processes

Cited by John A Sciacchitano

21 Nov 2019
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by John A Sciacchitano

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 observations4x
21 CFR 820.70(i)Cited across public-safe Form 483 observations4x

Full 483 report

Get the verbatim text of all 8 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