FDA inspection
Aurora Pharmaceutical, Inc.: FDA inspection ending Nov 27, 2018
FDA inspection 1075565 · No Action Indicated (NAI) · Northfield, MN
Key facts
| Inspection ID | 1075565 |
|---|---|
| Firm | Aurora Pharmaceutical, Inc. |
| FEI number | 3008276347 |
| Address | 1196 Highway 3 S |
| City | Northfield |
| State | MN |
| ZIP | 55057 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Nov 27, 2018 |
| 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