FDA Inspection 1119726 — Mizuho America, Inc.

Mizuho America, Inc. — FEI 1000159388

The FDA completed an inspection of Mizuho America, Inc. on December 17, 2019 in Union City, CA. 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
December 17, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Union City, CA (United States)