FDA inspection

Synthon Argentina, SA: FDA inspection ending Dec 7, 2012

FDA inspection 813048 · Voluntary Action Indicated (VAI) · San Lorenzo

Key facts

Inspection ID 813048
Firm Synthon Argentina, SA
FEI number 3005619726
Address Ruta Nacional 11 Km 325
City San Lorenzo
Country Argentina
Fiscal year 2013
Inspection end date Dec 7, 2012
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None 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

Browse all FDA inspections