FDA inspection

Takeda GmbH: FDA inspection ending Jun 10, 2009

FDA inspection 595522 · Voluntary Action Indicated (VAI) · Singen (Hohentwiel)

Key facts

Inspection ID 595522
Firm Takeda GmbH
FEI number 3002806542
Address Robert-Bosch-Str. 8
City Singen (Hohentwiel)
Country Germany
Fiscal year 2009
Inspection end date Jun 10, 2009
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

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
  • 10–99 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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