FDA inspection

Dr. Japan Co., Ltd.: FDA inspection ending Jun 28, 2015

FDA inspection 933520 · Voluntary Action Indicated (VAI) · Gyoda

Key facts

Inspection ID 933520
Firm Dr. Japan Co., Ltd.
FEI number 3009384766
Address 4 Chome 15-1, Nagano
City Gyoda
Country Japan
Fiscal year 2015
Inspection end date Jun 28, 2015
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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