# FDA Inspection 932660 - Philips North  America, LLC - June 18, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/philips-north-america-llc/9d36fe95-670f-4894-8c09-bb9a0629541d
Source feed: FDA_Inspections

> FDA Inspection 932660 for Philips North  America, LLC on June 18, 2015. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 932660
- Company Name: Philips North  America, LLC
- Inspection Date: 2015-06-18
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: 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/79612d5c-f4a6-4cc1-8134-f23502db5bf9

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