FDA inspection

Mizuho America, Inc.: FDA inspection ending Dec 17, 2019

FDA inspection 1119726 · No Action Indicated (NAI) · Union City, CA

Key facts

Inspection ID 1119726
Firm Mizuho America, Inc.
FEI number 1000159388
Address 30057 Ahern Ave
City Union City
State CA
ZIP 94587
Country United States
Fiscal year 2020
Inspection end date Dec 17, 2019
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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