Xu Zhou Vimed Nonwoven Co., Ltd. – FDA Inspection, Apr 6, 2017

Record Details

This FDA Inspection record concerns Xu Zhou Vimed Nonwoven Co., Ltd., with an inspection on April 6, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Xu Zhou Vimed Nonwoven Co., Ltd.
Inspection Date: April 6, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health
Person: Stephen D. Eich (Company Rep)

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ID · 6474705a-e8a5-4180-ab00-e7ff93d4aa67

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number: 1010519
FDA center: Medical Devices & Rad Health
Project area: Compliance: Devices
Outcome: Form 483 issued

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FDA Inspection

Xu Zhou Vimed Nonwoven Co., Ltd.April 6, 2017