# FDA Inspection 923916 - Philips North America LLC - April 21, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/philips-north-america-llc/dd22636e-8452-4876-b3c4-b8ffe7523737
Source feed: FDA_Inspections

> FDA Inspection 923916 for Philips North America LLC on April 21, 2015. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 923916
- Company Name: Philips North America LLC
- Inspection Date: 2015-04-21
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- 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/d7335702-bc34-4fb8-acdc-db91e81d2f8c

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