Form 483

Laboratorios Leon Farma SAU Form 483, 2018-05-25

FDA issued a Form 483 to Laboratorios Leon Farma SAU on 2018-05-25 with 2 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health2 observations

Laboratorios Leon Farma SAU · Villaquilambre, Spain · Issued May 25, 2018

Overview

  • 2 public-safe observations are available for this inspection.
  • 1 structured CFR citation is represented.
  • 3 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

25 May 2018
21 CFR 820.30(a)

Design control - no procedures

Cited by Seema S Singh, Michael L Casner, James Norman

25 May 2018
21 CFR 820.30(a)

Design control - no procedures

Cited by Seema S Singh, Michael L Casner, James Norman

Inspected site

LLLaboratorios Leon Farma SAUVillaquilambre, Spain

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.30(a)Cited across public-safe Form 483 observations2x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 2 observations

The source PDF, 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