Form 483

Lambda SpA Form 483, 2023-10-19

FDA issued a Form 483 to Lambda SpA on 2023-10-19 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Lambda SpA · Brendola, Italy · Issued October 19, 2023

Overview

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

19 Oct 2023
21 CFR 820.120

Lack of or inadequate procedures for labeling

Cited by Gamal A Norton

19 Oct 2023
21 CFR 820.50(a)(1)

Documented evaluation

Cited by Gamal A Norton

19 Oct 2023
21 CFR 820.75(a)

Documentation

Cited by Gamal A Norton

19 Oct 2023
21 CFR 820.80(c)

Lack of or inadequate In-process acceptance procedures

Cited by Gamal A Norton

Inspected site

LSLambda SpABrendola, Italy

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.120Cited across public-safe Form 483 observations1x
21 CFR 820.50(a)(1)Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x
21 CFR 820.80(c)Cited across public-safe Form 483 observations1x

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