# FDA Inspection 883572 - LHI Technology (Shenzhen) Co., Ltd. - May 15, 2014

Source: https://www.keypedia.com/records/fda_inspections/lhi-technology-shenzhen-co-ltd/18393ba0-e7ac-4e20-bc87-913c73d417c5
Source feed: FDA_Inspections

> FDA Inspection 883572 for LHI Technology (Shenzhen) Co., Ltd. on May 15, 2014. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 883572
- Company Name: LHI Technology (Shenzhen) Co., Ltd.
- Inspection Date: 2014-05-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 883572 - 2014-05-15](https://www.keypedia.com/records/fda_inspections/lhi-technology-shenzhen-co-ltd/461b7431-0a95-4d36-9580-a0edf9696ef9)

Company: https://www.keypedia.com/companies/lhi-technology-shenzhen-co-ltd/50fa53af-6691-4eee-a362-395620cf7cd7

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