# Philips Medical Systems DMC GmbH – FDA Inspection, Jun 14, 2013

Source: https://www.keypedia.com/records/fda_inspections/philips-medical-systems-dmc-gmbh/bcc90121-b5c9-4e5f-94f0-87c2dcf8130a
Source feed: FDA_Inspections

> FDA inspection 843790 of Philips Medical Systems DMC GmbH, June 14, 2013. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 843790
- Company Name: Philips Medical Systems DMC GmbH
- Inspection Date: 2013-06-14
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- 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: 0

## Related Documents

- [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

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