FDA inspection

TERUMO CORPORATION: FDA inspection ending Apr 17, 2014

FDA inspection 877631 · No Action Indicated (NAI) · Nakakoma-Gun

Key facts

Inspection ID 877631
Firm TERUMO CORPORATION
FEI number 3003752255
Address 1727-1, Tsuijiarai; Showa-Cho
City Nakakoma-Gun
Country Japan
Fiscal year 2014
Inspection end date Apr 17, 2014
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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