FDA inspection

Aizu Olympus Co., Ltd.: FDA inspection ending Apr 17, 2015

FDA inspection 925884 · Voluntary Action Indicated (VAI) · Aizuwakamatsu

Key facts

Inspection ID 925884
Firm Aizu Olympus Co., Ltd.
FEI number 3002964398
Address 500, Mondenmachioazaniidera
City Aizuwakamatsu
Country Japan
Fiscal year 2015
Inspection end date Apr 17, 2015
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 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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