FDA inspection

Nikkiso Ltd - Shizuoka Plant: FDA inspection ending Feb 22, 2016

FDA inspection 963499 · No Action Indicated (NAI) · Makinohara

Key facts

Inspection ID 963499
Firm Nikkiso Ltd - Shizuoka Plant
FEI number 3002807721
Address Hibataso ( Kabu ) Shizuokaseisakusho, Makinohara-shi
City Makinohara
Country Japan
Fiscal year 2016
Inspection end date Feb 22, 2016
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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