# Philips Medical Systems DMC GmbH – FDA Inspection, Jan 19, 2023

Source: https://www.keypedia.com/records/fda_inspections/philips-medical-systems-dmc-gmbh/87215a9b-73e8-4ab2-95be-6f4a5f11951c
Source feed: FDA_Inspections

> FDA inspection 1195414 of Philips Medical Systems DMC GmbH, January 19, 2023. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 806 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 933942 - 2015-07-09
- [FDA Inspection 843790 - 2013-06-14](https://www.keypedia.com/records/fda_inspections/philips-medical-systems-dmc-gmbh/bcc90121-b5c9-4e5f-94f0-87c2dcf8130a)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/janet-pulver/d46b01cd-8c3d-4a54-bb91-843e0f94de89)

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