FDA inspection

Machida Endoscope Co., Ltd.: FDA inspection ending Aug 23, 2017

FDA inspection 1030560 · No Action Indicated (NAI) · Abiko

Key facts

Inspection ID 1030560
Firm Machida Endoscope Co., Ltd.
FEI number 3002807522
Address Chiba Prefecture J, 15-12 Abiko 1 Chome; Abiko; Abiko; Abiko
City Abiko
Country Japan
Fiscal year 2017
Inspection end date Aug 23, 2017
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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