# FDA Inspection 860079 - Philips North  America, LLC - December 12, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/philips-north-america-llc/f74e4d68-9a73-4ef7-803d-9de447191c98/
Source feed: FDA_Inspections

> FDA Inspection 860079 for Philips North  America, LLC on December 12, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 860079
- Company Name: Philips North  America, LLC
- Inspection Date: 2013-12-12
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/philips-north-america-llc/79612d5c-f4a6-4cc1-8134-f23502db5bf9

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