Form 483

Laboratorios Leon Farma SAU Form 483, 2026-01-15

FDA issued a Form 483 to Laboratorios Leon Farma SAU on 2026-01-15 with 2 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health2 observations

Laboratorios Leon Farma SAU · Villaquilambre, Spain · Issued January 15, 2026

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.

15 Jan 2026
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Joshua J Silvestri

15 Jan 2026
21 CFR 820.30(a)

Design control - no procedures

Cited by Joshua J Silvestri

Inspected site

LLLaboratorios Leon Farma SAUVillaquilambre, Spain

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.30(a)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