FDA inspection
Kolmar Korea Co., Ltd. Bucheon Factory: FDA inspection ending Mar 22, 2019
FDA inspection 1087335 · No Action Indicated (NAI) · Bucheon
Key facts
| Inspection ID | 1087335 |
|---|---|
| Firm | Kolmar Korea Co., Ltd. Bucheon Factory |
| FEI number | 3010818961 |
| Address | 157 Pyeongcheonro850beon-Gil |
| City | Bucheon |
| Country | Korea (the Republic of) |
| Fiscal year | 2019 |
| Inspection end date | Mar 22, 2019 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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