FDA inspection

Hans Biomed Corporation: FDA inspection ending Apr 5, 2019

FDA inspection 1091073 · No Action Indicated (NAI) · Yuseong District

Key facts

Inspection ID 1091073
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 2019
Inspection end date Apr 5, 2019
Classification No Action Indicated (NAI)
Project area Human Cellular, Tissue, and Gene Therapies
Product type Biologics

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

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