FDA Inspection 1030560 — Machida Endoscope Co., Ltd.

Machida Endoscope Co., Ltd. — FEI 3002807522

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.