FDA inspection

Geistlich Pharma AG: FDA inspection ending Feb 12, 2009

FDA inspection 563924 · Voluntary Action Indicated (VAI) · Wolhusen

Key facts

Inspection ID 563924
Firm Geistlich Pharma AG
FEI number 3000303710
Address Bahnhofstrasse 40
City Wolhusen
Country Switzerland
Fiscal year 2009
Inspection end date Feb 12, 2009
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

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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