FDA inspection

Recipharm Leganes SLU: FDA inspection ending Feb 5, 2010

FDA inspection 651878 · Voluntary Action Indicated (VAI) · Leganes

Key facts

Inspection ID 651878
Firm Recipharm Leganes SLU
FEI number 3000298591
Address Calle De Severo Ochoa 13
City Leganes
Country Spain
Fiscal year 2010
Inspection end date Feb 5, 2010
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type 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
  • 1–9 Inspections at this FEI

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

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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