FDA inspection

Taiho Pharmaceutical Co., Ltd.: FDA inspection ending May 22, 2015

FDA inspection 930223 · No Action Indicated (NAI) · Itano-Gun

Key facts

Inspection ID 930223
Firm Taiho Pharmaceutical Co., Ltd.
FEI number 3010872322
Address Iuchi 1-1, Takabo; Kitajima-Cho
City Itano-Gun
Country Japan
Fiscal year 2015
Inspection end date May 22, 2015
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None 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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