# Philips IntelliSpace Event Management – FDA Inspection, Jul 18, 2013

Source: https://www.keypedia.com/records/fda_inspections/philips-intellispace-event-management/6a1458ed-cc82-4c59-afc6-df6cca1b33e5
Source feed: FDA_Inspections

> FDA inspection 841413 of Philips IntelliSpace Event Management, July 18, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 841413
- Company Name: Philips IntelliSpace Event Management
- Inspection Date: 2013-07-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

Company: https://www.keypedia.com/companies/philips-intellispace-event-management/1ae494f6-f282-4363-b049-4ce930b67ce2

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