FDA inspection
Samsung Bioepis Co., Ltd.: FDA inspection ending Aug 19, 2016
FDA inspection 988922 · Voluntary Action Indicated (VAI) · Yeonsu
Key facts
| Inspection ID | 988922 |
|---|---|
| Firm | Samsung Bioepis Co., Ltd. |
| FEI number | 3010031951 |
| Address | Samseongbaioepiseu(Ju), Cheomdandae-Ro 107/107 |
| City | Yeonsu |
| Country | Korea (the Republic of) |
| Fiscal year | 2016 |
| Inspection end date | Aug 19, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 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