# FDA Inspection 942438 - Philips Goldway (Shenzhen) Industrial, Inc. - July 30, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/philips-goldway-shenzhen-industrial-inc/04abe639-98fb-485b-b425-ebb3b2a96a90
Source feed: FDA_Inspections

> FDA Inspection 942438 for Philips Goldway (Shenzhen) Industrial, Inc. on July 30, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 942438
- Company Name: Philips Goldway (Shenzhen) Industrial, Inc.
- Inspection Date: 2015-07-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/philips-goldway-shenzhen-industrial-inc/d899ad7a-4efa-4c69-8405-fce6b5d50b8d

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