FDA Inspection 1030560 — Machida Endoscope Co., Ltd.

Machida Endoscope Co., Ltd. — FEI 3002807522

The FDA completed an inspection of Machida Endoscope Co., Ltd. on August 23, 2017 in Abiko. 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
August 23, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Abiko (Japan)