FDA Inspection 951728 — Asahi Kasei Medical Co., Ltd.

Asahi Kasei Medical Co., Ltd. — FEI 3009960884

The FDA completed an inspection of Asahi Kasei Medical Co., Ltd. on Dec 9, 2015 in Chiyoda. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 9, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Chiyoda (Japan)