FDA inspection
Thymoorgan Pharmazie Gmbh: FDA inspection ending Dec 16, 2016
FDA inspection 1003153 · No Action Indicated (NAI) · Goslar
Key facts
| Inspection ID | 1003153 |
|---|---|
| Firm | Thymoorgan Pharmazie Gmbh |
| FEI number | 3002320821 |
| Address | Schiffgraben 23 |
| City | Goslar |
| Country | Germany |
| Fiscal year | 2017 |
| Inspection end date | Dec 16, 2016 |
| 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