# FDA Inspection 598802 - Pierre P Leimgruber MD - June 25, 2009

Source: https://www.keypedia.com/records/fda_inspections/pierre-p-leimgruber-md/14e7e54e-2246-4d88-8f5d-88d2fd5ca2a9
Source feed: FDA_Inspections

> FDA Inspection 598802 for Pierre P Leimgruber MD on June 25, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 598802
- Company Name: Pierre P Leimgruber MD
- Inspection Date: 2009-06-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/pierre-p-leimgruber-md/d939171d-e6a9-4c45-930e-f92fce440856

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