Form 483

Peter Lazic Gmbh Form 483, 2024-04-05

FDA issued a Form 483 to Peter Lazic Gmbh on 2024-04-05 with 2 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health2 observations

Peter Lazic Gmbh · Tuttlingen, Germany · Issued April 5, 2024

Overview

  • 2 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.

5 Apr 2024
21 CFR 803.50(a)(2)

Individual Report of Malfunction

Cited by Jude C Dike

5 Apr 2024
21 CFR 820.30(j)

Design history file

Cited by Jude C Dike

Inspected site

PLPeter Lazic GmbhTuttlingen, Germany

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.50(a)(2)Cited across public-safe Form 483 observations1x
21 CFR 820.30(j)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 2 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