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

Record Details

This FDA Inspection record concerns Hangzhou AGS Meditech Co., Ltd., with an inspection on May 2, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Hangzhou AGS Meditech Co., Ltd.
Inspection Date: May 2, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health
Person: Stephen D. Eich (Company Rep)

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ID · da42403a-d6e6-4e7a-976b-ecf6379e8817

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number: 1091757
FDA center: Medical Devices & Rad Health
Project area: Postmarket Assurance: Devices
Outcome: Form 483 issued

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FDA Inspection

Hangzhou AGS Meditech Co., Ltd.May 2, 2019