FDA inspection
Daesung Maref Co., Ltd.: FDA inspection ending Jul 26, 2018
FDA inspection 1065659 · No Action Indicated (NAI) · Gunpo
Key facts
| Inspection ID | 1065659 |
|---|---|
| Firm | Daesung Maref Co., Ltd. |
| FEI number | 3004116008 |
| Address | 298-24 Gongdan-ro |
| City | Gunpo |
| Country | Korea (the Republic of) |
| Fiscal year | 2018 |
| Inspection end date | Jul 26, 2018 |
| 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