FDA inspection

Takeda Manufacturing Austria AG: FDA inspection ending Jan 28, 2010

FDA inspection 648799 · Voluntary Action Indicated (VAI) · Vienna

Key facts

Inspection ID 648799
Firm Takeda Manufacturing Austria AG
FEI number 3002807133
Address Industriestrase 131
City Vienna
Country Austria
Fiscal year 2010
Inspection end date Jan 28, 2010
Classification Voluntary Action Indicated (VAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • None 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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