FDA inspection

GE ULTRASOUND KOREA, LTD.: FDA inspection ending Nov 17, 2011

FDA inspection 756281 · No Action Indicated (NAI) · Seongnam

Key facts

Inspection ID 756281
Firm GE ULTRASOUND KOREA, LTD.
FEI number 3003208270
Address 9, Sunhwan-ro 214beon-gil, Jungwon-gu
City Seongnam
Country Korea (the Republic of)
Fiscal year 2012
Inspection end date Nov 17, 2011
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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