# FDA Inspection 1195414 - Philips Medical Systems DMC GmbH - January 19, 2023

Source: https://www.keypedia.com/records/fda_inspections/philips-medical-systems-dmc-gmbh/43ba38be-3d63-4e98-8de1-862e122d7e0b
Source feed: FDA_Inspections

> FDA Inspection 1195414 for Philips Medical Systems DMC GmbH on January 19, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1195414
- Company Name: Philips Medical Systems DMC GmbH
- Inspection Date: 2023-01-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1195414 - 2023-01-19](https://www.keypedia.com/records/fda_inspections/philips-medical-systems-dmc-gmbh/4788eec8-71f5-4502-b2bc-2f2f7ce438bb)
- [FDA Inspection 1195414 - 2023-01-19](https://www.keypedia.com/records/fda_inspections/philips-medical-systems-dmc-gmbh/87215a9b-73e8-4ab2-95be-6f4a5f11951c)
- [FDA Inspection 933942 - 2015-07-09](https://www.keypedia.com/records/fda_inspections/philips-medical-systems-dmc-gmbh/5202d1f2-398b-42d4-a0aa-a8761c13edd1)
- [FDA Inspection 933942 - 2015-07-09](https://www.keypedia.com/records/fda_inspections/philips-medical-systems-dmc-gmbh/ba8c2768-be18-42f4-8565-3dc952a637a0)
- [FDA Inspection 843790 - 2013-06-14](https://www.keypedia.com/records/fda_inspections/philips-medical-systems-dmc-gmbh/bcc90121-b5c9-4e5f-94f0-87c2dcf8130a)

Company: https://www.keypedia.com/companies/philips-medical-systems-dmc-gmbh/78164a38-f997-43ff-8470-20686ac91ad1

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