FDA inspection

Hans Biomed Corporation: FDA inspection ending Mar 2, 2009

FDA inspection 575354 · No Action Indicated (NAI) · Yuseong District

Key facts

Inspection ID 575354
Firm Hans Biomed Corporation
FEI number 3003828812
Address Youseong, 64 Yuseong-Daero 1628 Beon-Gil
City Yuseong District
Country Korea (the Republic of)
Fiscal year 2009
Inspection end date Mar 2, 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
  • 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

Browse all FDA inspections