FDA inspection
Nordmark Pharma GmbH: FDA inspection ending Nov 20, 2014
FDA inspection 907095 · Voluntary Action Indicated (VAI) · Uetersen
Key facts
| Inspection ID | 907095 |
|---|---|
| Firm | Nordmark Pharma GmbH |
| FEI number | 3003293533 |
| Address | Pinnauallee 4 |
| City | Uetersen |
| Country | Germany |
| Fiscal year | 2015 |
| Inspection end date | Nov 20, 2014 |
| 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