FDA inspection
Recipharm Uppsala AB: FDA inspection ending Mar 14, 2014
FDA inspection 869566 · Voluntary Action Indicated (VAI) · Uppsala
Key facts
| Inspection ID | 869566 |
|---|---|
| Firm | Recipharm Uppsala AB |
| FEI number | 1000171246 |
| Address | Bjorkgatan 30 |
| City | Uppsala |
| Country | Sweden |
| Fiscal year | 2014 |
| Inspection end date | Mar 14, 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