FDA Inspection 1050806 — Omron Healthcare Co., Ltd

Omron Healthcare Co., Ltd — FEI 3002807674

The FDA completed an inspection of Omron Healthcare Co., Ltd on Mar 2, 2018 in Matsusaka. 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 2, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Matsusaka (Japan)

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