# FDA Inspection 930331 - Philippe Laberge, MD - December 12, 2014

Source: https://www.keypedia.com/records/fda_inspections/philippe-laberge-md/7a49e832-ca96-4a6f-8cff-33400961913a
Source feed: FDA_Inspections

> FDA Inspection 930331 for Philippe Laberge, MD on December 12, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 930331
- Company Name: Philippe Laberge, MD
- Inspection Date: 2014-12-12
- 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/philippe-laberge-md/bdcb1618-d674-4b14-8fd7-7616bd80a92f

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