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FDA inspection

Laboratorios Leon Farma SAU: FDA inspection ending May 25, 2018

FDA inspection 1053237 · No Action Indicated (NAI) · Navatejera

Key facts

Inspection ID 1053237
Firm Laboratorios Leon Farma SAU
FEI number 3006188375
Address Poligono Industrial Navatejera, Calle La Vallina
City Navatejera
Fiscal year 2018
Inspection end date May 25, 2018
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation
Product type Devices, Drugs

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

Other inspections at this establishment

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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