FDA inspection

Toyobo Co. Ltd.: FDA inspection ending Feb 25, 2021

FDA inspection 1136484 · Official Action Indicated (OAI) · Otsu

Key facts

Inspection ID 1136484
Firm Toyobo Co. Ltd.
FEI number 1000251214
Address Toyobo (Kabu) Sogokenkyusho, 2 Chome Sogokenkyusho; Katata
City Otsu
Country Japan
Fiscal year 2021
Inspection end date Feb 25, 2021
Classification Official Action Indicated (OAI)
Project area Drug Quality Assurance
Product type Drugs
Warning letter 614177

At a glance

  • 10–99 Citations
  • 1–9 Posted citations
  • Yes 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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