# FDA Inspection 1059711 - Philips Commercial France SAS - July 12, 2018

Source: https://www.keypedia.com/records/fda_inspections/philips-commercial-france-sas/a71494d0-0046-49db-92f1-16a305e08a4c
Source feed: FDA_Inspections

> FDA Inspection 1059711 for Philips Commercial France SAS on July 12, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1059711
- Company Name: Philips Commercial France SAS
- Inspection Date: 2018-07-12
- 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/philips-commercial-france-sas/f2f470d1-b435-465e-989c-f49055844316

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