# FDA Inspection 563924 - Geistlich Pharma AG - February 12, 2009

Source: https://www.keypedia.com/records/fda_inspections/geistlich-pharma-ag/ef5830b1-f3ad-4ef8-b9a6-607118e8e10d
Source feed: FDA_Inspections

> FDA Inspection 563924 for Geistlich Pharma AG on February 12, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 563924
- Company Name: Geistlich Pharma AG
- Inspection Date: 2009-02-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/geistlich-pharma-ag/ab59375a-0018-4a17-a333-214a4f2733cb

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7