# FDA Inspection 1208824 - HUREV Co., Ltd. - June 02, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/hurev-co-ltd/1f93d720-686d-4c90-99c3-38346017c31c
Source feed: FDA_Inspections

> FDA Inspection 1208824 for HUREV Co., Ltd. on June 02, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1208824
- Company Name: HUREV Co., Ltd.
- Inspection Date: 2023-06-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1208824 - 2023-06-02](https://www.globalkeysolutions.net/records/fda_inspections/hurev-co-ltd/086667e7-784f-429a-8a9b-6858f2ac4848)
- [FDA Inspection 1115962 - 2020-01-17](https://www.globalkeysolutions.net/records/fda_inspections/hurev-co-ltd/5c73f521-838c-45cd-8f2f-a3a43b312ec9)
- [FDA Inspection 1115962 - 2020-01-17](https://www.globalkeysolutions.net/records/fda_inspections/hurev-co-ltd/86b4adac-1e12-48f5-af94-9db74a187e71)
- [FDA Inspection 1019051 - 2017-06-29](https://www.globalkeysolutions.net/records/fda_inspections/hurev-co-ltd/f6dc6bc0-5567-44f4-a535-1ba90865fd2f)

Company: https://www.globalkeysolutions.net/companies/hurev-co-ltd/03777eca-a22e-40bb-9908-83826810103f

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