# Philips North  America, LLC – FDA Inspection, Dec 12, 2013

Source: https://www.keypedia.com/records/fda_inspections/philips-north-america-llc/c1d1a994-e3aa-49d0-af85-5b430baa3b38
Source feed: FDA_Inspections

> FDA inspection 860079 of Philips North  America, LLC, December 12, 2013. Classification: Official Action Indicated (OAI). 8 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 860079
- Company Name: Philips North  America, LLC
- Inspection Date: 2013-12-12
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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

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