# FDA Inspection 841413 - Philips IntelliSpace Event Management - July 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 for Philips IntelliSpace Event Management on July 18, 2013. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 841413 - 2013-07-18](https://www.keypedia.com/records/fda_inspections/philips-intellispace-event-management/37c1ff61-6692-45b9-8dcc-1194f55b06ff)

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