Nenesupply Co., Ltd. – FDA Inspection, Jan 24, 2017

Record Details

This FDA Inspection record concerns Nenesupply Co., Ltd., with an inspection on January 24, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Nenesupply Co., Ltd.
Inspection Date: January 24, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health
Person: Nicholas C Mendiola (Issuing Officer)

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ID · 4ce06045-c460-4a74-9626-993691807483

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number: 1001748
FDA center: Medical Devices & Rad Health
Project area: Postmarket Assurance: Devices
Outcome: Form 483 issued

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FDA Inspection

Nenesupply Co., Ltd.January 24, 2017