FDA inspection

Omron Healthcare Co., Ltd: FDA inspection ending Mar 2, 2018

FDA inspection 1050806 · No Action Indicated (NAI) · Matsusaka

Key facts

Inspection ID 1050806
Firm Omron Healthcare Co., Ltd
FEI number 3002807674
Address Omuronherusukea (Kabu) Matsusakajigyosho, 1855-370; Kubo-Cho
City Matsusaka
Country Japan
Fiscal year 2018
Inspection end date Mar 2, 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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