FDA Inspection 1050439 — TOSOH AIA, Inc.

TOSOH AIA, Inc. — FEI 3002808328

The FDA completed an inspection of TOSOH AIA, Inc. on Apr 12, 2018 in Toyama. 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
Apr 12, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Toyama (Japan)