# FDA 483 - Philips Goldway (Shenzhen) Industrial, Inc. - July 30, 2015

Source: https://www.globalkeysolutions.net/records/483/philips-goldway-shenzhen-industrial-inc/4a5bbe9c-26e4-4714-9cb8-738f7ebe7a76

> FDA 483 for Philips Goldway (Shenzhen) Industrial, Inc. on July 30, 2015. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Philips Goldway (Shenzhen) Industrial, Inc.
- Inspection Date: 2015-07-30
- Product Type: device
- Office Name: Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)

## Related Documents

- [483 - 2015-07-30](https://www.globalkeysolutions.net/records/483/philips-goldway-shenzhen-industrial-inc/818d8840-cb8d-4c0d-8d4f-2f8a8e996dad)

## Related Officers

- [Consumer Safety Officer](https://www.globalkeysolutions.net/people/catherine-j-laufmann/920b7656-2847-408d-ba15-3989283d8c94)

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

Office: https://www.globalkeysolutions.net/offices/division-of-clinical-evidence-and-analysis-1-clinical-policy-and-quality/5f95da17-30bb-423f-b892-5ea041823fbd