FDA inspection
Medicore Co., Ltd.: FDA inspection ending Apr 25, 2019
FDA inspection 1091675 · Voluntary Action Indicated (VAI) · Seongnam
Key facts
| Inspection ID | 1091675 |
|---|---|
| Firm | Medicore Co., Ltd. |
| FEI number | 2000010846 |
| Address | No. 801-803, Joonganginnotech, 148, Sagimakgolro, Jungwon-Gu |
| City | Seongnam |
| Country | Korea (the Republic of) |
| Fiscal year | 2019 |
| Inspection end date | Apr 25, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes 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