FDA inspection
Gedeon Richter Plc., Dorog Site: FDA inspection ending Feb 8, 2019
FDA inspection 1099017 · No Action Indicated (NAI) · Dorog
Key facts
| Inspection ID | 1099017 |
|---|---|
| Firm | Gedeon Richter Plc., Dorog Site |
| FEI number | 3002806762 |
| Address | H-2511 Dorog, Pf. 26, Esztergomi ut 27 |
| City | Dorog |
| Country | Hungary |
| Fiscal year | 2019 |
| Inspection end date | Feb 8, 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