FDA Inspection 1069144 — Anzai Medical Co., Ltd.

Anzai Medical Co., Ltd. — FEI 3008328959

The FDA completed an inspection of Anzai Medical Co., Ltd. on July 26, 2018 in Shinagawa. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 26, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Shinagawa (Japan)