FDA Inspection 1007018 — Sanjenics Inc.

Sanjenics Inc. — FEI 3013013401

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