# FDA Inspection 973310 - YANGZHONG MEDI TECH CO., LTD - May 12, 2016

Source: https://www.keypedia.com/records/fda_inspections/yangzhong-medi-tech-co-ltd/2d436169-ffe6-4ec2-8881-c70e35aefda0
Source feed: FDA_Inspections

> FDA Inspection 973310 for YANGZHONG MEDI TECH CO., LTD on May 12, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 973310
- Company Name: YANGZHONG MEDI TECH CO., LTD
- Inspection Date: 2016-05-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 973310 - 2016-05-12](https://www.keypedia.com/records/fda_inspections/yangzhong-medi-tech-co-ltd/b3a623ed-ae7c-45b1-b2f8-df7960041925)

Company: https://www.keypedia.com/companies/yangzhong-medi-tech-co-ltd/f79d12e8-2e3d-48b4-a05a-54129c8558c0

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