FDA Inspection 1051605 — Hogy Medical Co., Ltd.

Hogy Medical Co., Ltd. — FEI 3003624296

The FDA completed an inspection of Hogy Medical Co., Ltd. on Mar 28, 2018 in Ibaraki. 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
Mar 28, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Ibaraki (Japan)