# FDA Inspection 803386 - Philips Electronics Ltd. - September 13, 2012

Source: https://www.keypedia.com/records/fda_inspections/philips-electronics-ltd/d1aca044-534f-416a-a58b-c040d7bddfcb
Source feed: FDA_Inspections

> FDA Inspection 803386 for Philips Electronics Ltd. on September 13, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803386
- Company Name: Philips Electronics Ltd.
- Inspection Date: 2012-09-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 803386 - 2012-09-13](https://www.keypedia.com/records/fda_inspections/philips-electronics-ltd/8bae3eff-3e12-4f92-bd00-0ab915c66774)

Company: https://www.keypedia.com/companies/philips-electronics-ltd/c16ead46-bec4-4971-9a45-d54265ee30d8

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