Form 483

Peter Lazic Gmbh Form 483, 2017-05-18

FDA issued a Form 483 to Peter Lazic Gmbh on 2017-05-18 with 10 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health10 observations

Peter Lazic Gmbh · Tuttlingen, Germany · Issued May 18, 2017

Overview

  • 10 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.

18 May 2017
21 CFR 820.100(b)

Documentation

Cited by Benjamin J Dastoli

18 May 2017
21 CFR 820.100(b)

Documentation

Cited by Benjamin J Dastoli

18 May 2017
21 CFR 820.30(g)

Design Validation - Risk analysis not performed/inadequate

Cited by Benjamin J Dastoli

18 May 2017
21 CFR 820.30(g)

Design Validation - Risk analysis not performed/inadequate

Cited by Benjamin J Dastoli

18 May 2017
21 CFR 820.40

Procedures not adequately established or maintained

Cited by Benjamin J Dastoli

Inspected site

PLPeter Lazic GmbhTuttlingen, 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 observations2x
21 CFR 820.30(g)Cited across public-safe Form 483 observations2x
21 CFR 820.40Cited across public-safe Form 483 observations2x
21 CFR 820.50(a)(2)Cited across public-safe Form 483 observations2x
21 CFR 820.90(a)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 10 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