FDA inspection

Siemens Healthineers Ltd.: FDA inspection ending May 21, 2009

FDA inspection 592784 · No Action Indicated (NAI) · Seongnam

Key facts

Inspection ID 592784
Firm Siemens Healthineers Ltd.
FEI number 3002619337
Address Kins Tower, 8, 331beon-gil, Bundang-gu
City Seongnam
Country Korea (the Republic of)
Fiscal year 2009
Inspection end date May 21, 2009
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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