# FDA Inspection 1023742 - Philips Electronics North America Corporation - August 31, 2017

Source: https://www.keypedia.com/records/fda_inspections/philips-electronics-north-america-corporation/56c2211c-c458-408e-ba51-7b5ff957c607
Source feed: FDA_Inspections

> FDA Inspection 1023742 for Philips Electronics North America Corporation on August 31, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023742
- Company Name: Philips Electronics North America Corporation
- Inspection Date: 2017-08-31
- 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 1023742 - 2017-08-31](https://www.keypedia.com/records/fda_inspections/philips-electronics-north-america-corporation/d19a8b7e-1f44-4797-be5d-23749eb13383)
- [FDA Inspection 806265 - 2012-10-30](https://www.keypedia.com/records/fda_inspections/philips-electronics-north-america-corporation/31936223-cc7c-4788-aa9a-04a50fc86849)

Company: https://www.keypedia.com/companies/philips-electronics-north-america-corporation/6b6a3065-ebd6-47df-86a7-ced067e5bb9d

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