# FDA Inspection 1091757 - Hangzhou AGS Meditech Co., Ltd. - May 02, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/hangzhou-ags-meditech-co-ltd/da42403a-d6e6-4e7a-976b-ecf6379e8817
Source feed: FDA_Inspections

> FDA Inspection 1091757 for Hangzhou AGS Meditech Co., Ltd. on May 02, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1091757
- Company Name: Hangzhou AGS Meditech Co., Ltd.
- Inspection Date: 2019-05-02
- 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 1091757 - 2019-05-02](https://www.globalkeysolutions.net/records/fda_inspections/hangzhou-ags-meditech-co-ltd/b8148865-7cf9-4bcb-bab7-d67d3b6e3b0a)

Company: https://www.globalkeysolutions.net/companies/hangzhou-ags-meditech-co-ltd/a3e3b5bc-6e88-4591-b754-7aa5370e8ce6

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