FDA inspection

Gedeon Richter Nyrt.: FDA inspection ending Jul 12, 2011

FDA inspection 738485 · Voluntary Action Indicated (VAI) · Budapest

Key facts

Inspection ID 738485
Firm Gedeon Richter Nyrt.
FEI number 3002806761
Address Gyomroi ut 19-21
City Budapest
Country Hungary
Fiscal year 2011
Inspection end date Jul 12, 2011
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

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