# FDA Inspection 987018 - Shi Heng Technology Co., Ltd. - August 25, 2016

Source: https://www.keypedia.com/records/fda_inspections/shi-heng-technology-co-ltd/d4d24de9-2e08-4e8d-8a64-b75281e64f76
Source feed: FDA_Inspections

> FDA Inspection 987018 for Shi Heng Technology Co., Ltd. on August 25, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 987018
- Company Name: Shi Heng Technology Co., Ltd.
- Inspection Date: 2016-08-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 987018 - 2016-08-25](https://www.keypedia.com/records/fda_inspections/shi-heng-technology-co-ltd/c61d1bdd-5228-4893-8e92-f6fab5916a7d)

Company: https://www.keypedia.com/companies/shi-heng-technology-co-ltd/8ceacd61-f69a-4f9d-9ca6-693f66f83726

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