FDA inspection

FUJINOMIYA FACTORY OF TERUMO CORP: FDA inspection ending May 19, 2023

FDA inspection 1206261 · Fujinomiya

Key facts

Inspection ID 1206261
Firm FUJINOMIYA FACTORY OF TERUMO CORP
FEI number 3002808337
Address 818, Misonodaira
City Fujinomiya
Fiscal year 2023
Inspection end date May 19, 2023
Project area Blood and Blood Products
Product type Biologics

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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