# FDA Inspection 903388 - Paul-Antoine Lehur, MD - October 15, 2014

Source: https://www.keypedia.com/records/fda_inspections/paul-antoine-lehur-md/27a166eb-114c-4a28-aaec-e1ea42ae7d11
Source feed: FDA_Inspections

> FDA Inspection 903388 for Paul-Antoine Lehur, MD on October 15, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 903388
- Company Name: Paul-Antoine Lehur, MD
- Inspection Date: 2014-10-15
- 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/paul-antoine-lehur-md/08557fcc-195c-4ab7-ba64-74639e72400c

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