FDA Inspection 1007018 — Sanjenics Inc.

Sanjenics Inc. — FEI 3013013401

The FDA completed an inspection of Sanjenics Inc. on Feb 2, 2017 in Nanto. 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
Feb 2, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Nanto (Japan)

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