Nihon Seimitsu Sokki Co., Ltd. – FDA Inspection, Dec 20, 2017

Record Details

This FDA Inspection record concerns Nihon Seimitsu Sokki Co., Ltd., with an inspection on December 20, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.

Company: Nihon Seimitsu Sokki Co., Ltd.
Inspection Date: December 20, 2017
Product Type: Medical Devices & Rad Health
Office: Office of Inspections and Investigations
Person: Roy Baby (Company Rep)

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ID · ba5235e4-0c41-400d-9ebc-0ee9662516aa

Inspection Facts

Inspection number: 1037787
FDA center: Medical Devices & Rad Health
Outcome: Form 483 issued

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FDA Inspection

Nihon Seimitsu Sokki Co., Ltd.December 20, 2017