FDA inspection
Haupt Pharma Muenster GmbH: FDA inspection ending Jul 6, 2018
FDA inspection 1059379 · Voluntary Action Indicated (VAI) · Munster
Key facts
| Inspection ID | 1059379 |
|---|---|
| Firm | Haupt Pharma Muenster GmbH |
| FEI number | 3006010798 |
| Address | Schleebruggenkamp 15 |
| City | Munster |
| Country | Germany |
| Fiscal year | 2018 |
| Inspection end date | Jul 6, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- 1–9 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