FDA inspection

Hogy Medical Co., Ltd.: FDA inspection ending Mar 28, 2018

FDA inspection 1051605 · No Action Indicated (NAI) · Ibaraki

Key facts

Inspection ID 1051605
Firm Hogy Medical Co., Ltd.
FEI number 3003624296
Address 1650-30 Okubara-Cho Ushiku
City Ibaraki
Country Japan
Fiscal year 2018
Inspection end date Mar 28, 2018
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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