FDA inspection

Gedeon Richter Nyrt.: FDA inspection ending Mar 3, 2017

FDA inspection 1009633 · No Action Indicated (NAI) · Budapest

Key facts

Inspection ID 1009633
Firm Gedeon Richter Nyrt.
FEI number 3002806761
Address Gyomroi ut 19-21
City Budapest
Country Hungary
Fiscal year 2017
Inspection end date Mar 3, 2017
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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