FDA inspection

Geistlich Pharma AG: FDA inspection ending Jun 22, 2017

FDA inspection 1031529 · Voluntary Action Indicated (VAI) · Wolhusen

Key facts

Inspection ID 1031529
Firm Geistlich Pharma AG
FEI number 3000303710
Address Bahnhofstrasse 40
City Wolhusen
Fiscal year 2017
Inspection end date Jun 22, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Medical 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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