# FDA Inspection 801911 - Philips Medical Systems Puerto Rico, Inc. - September 28, 2012

Source: https://www.keypedia.com/records/fda_inspections/philips-medical-systems-puerto-rico-inc/856b8d58-6221-4492-a54e-9ea816ed1868
Source feed: FDA_Inspections

> FDA Inspection 801911 for Philips Medical Systems Puerto Rico, Inc. on September 28, 2012. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 801911
- Company Name: Philips Medical Systems Puerto Rico, Inc.
- Inspection Date: 2012-09-28
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 986179 - 2016-09-13](https://www.keypedia.com/records/fda_inspections/philips-medical-systems-puerto-rico-inc/3d8fddf7-6376-47a6-a147-33dff3e320e2)
- [FDA Inspection 801911 - 2012-09-28](https://www.keypedia.com/records/fda_inspections/philips-medical-systems-puerto-rico-inc/4ae724c7-227f-41de-80cd-1b5baea976ec)

Company: https://www.keypedia.com/companies/philips-medical-systems-puerto-rico-inc/98de5d54-4694-4c64-b9f8-8759a4f9cc2e

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