# FDA Inspection 827925 - Philips Electronics North America Corporation - April 17, 2013

Source: https://www.keypedia.com/records/fda_inspections/philips-electronics-north-america-corporation/1ea94667-5f81-421b-a0ac-38d2c1a177d3
Source feed: FDA_Inspections

> FDA Inspection 827925 for Philips Electronics North America Corporation on April 17, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 827925
- Company Name: Philips Electronics North America Corporation
- Inspection Date: 2013-04-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/philips-electronics-north-america-corporation/3d3324d9-b010-4ff3-a200-ba9f247b1833

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