FDA inspection

Samsung Bioepis Co., Ltd.: FDA inspection ending Mar 7, 2018

FDA inspection 1046814 · No Action Indicated (NAI) · Yeonsu

Key facts

Inspection ID 1046814
Firm Samsung Bioepis Co., Ltd.
FEI number 3010031951
Address 76 Songdogyoyuk -Ro
City Yeonsu
Fiscal year 2018
Inspection end date Mar 7, 2018
Classification No Action Indicated (NAI)
Project area Generic Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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