FDA inspection

Nikkiso Ltd - Shizuoka Plant: FDA inspection ending Mar 7, 2013

FDA inspection 826373 · Voluntary Action Indicated (VAI) · Makinohara

Key facts

Inspection ID 826373
Firm Nikkiso Ltd - Shizuoka Plant
FEI number 3002807721
Address 498 1, Shizutani; Shizuoka-Ken
City Makinohara
Country Japan
Fiscal year 2013
Inspection end date Mar 7, 2013
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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