FDA inspection
Haupt Pharma Amareg GmbH: FDA inspection ending Nov 22, 2013
FDA inspection 857318 · No Action Indicated (NAI) · Ratisbon
Key facts
| Inspection ID | 857318 |
|---|---|
| Firm | Haupt Pharma Amareg GmbH |
| FEI number | 3008293991 |
| Address | Donaustaufer Str. 378 |
| City | Ratisbon |
| Country | Germany |
| Fiscal year | 2014 |
| Inspection end date | Nov 22, 2013 |
| 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