# FDA Inspection 974929 - Bureau Veritas Shenzhen Co., Ltd. - December 16, 2015

Source: https://www.keypedia.com/records/fda_inspections/bureau-veritas-shenzhen-co-ltd/c526e8d0-ae9f-47dc-ba9a-e34d22da7c81
Source feed: FDA_Inspections

> FDA Inspection 974929 for Bureau Veritas Shenzhen Co., Ltd. on December 16, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 974929
- Company Name: Bureau Veritas Shenzhen Co., Ltd.
- Inspection Date: 2015-12-16
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/bureau-veritas-shenzhen-co-ltd/6725fded-4502-4320-af62-7fb49f645cc9

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