# Hangzhou AGS Meditech Co., Ltd. – FDA Inspection, May 2, 2019

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

> FDA inspection 1091757 of Hangzhou AGS Meditech Co., Ltd., May 02, 2019. Classification: Voluntary Action Indicated (VAI). Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephen-d-eich/a932e816-cbe3-4f1c-84e7-8a81cc8b529e)

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

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