FDA inspection
Novo Nordisk US Bio Production Inc.: FDA inspection ending Mar 5, 2025
FDA inspection 1255809 · No Action Indicated (NAI) · West Lebanon, NH
Key facts
| Inspection ID | 1255809 |
|---|---|
| Firm | Novo Nordisk US Bio Production Inc. |
| FEI number | 3012593913 |
| Address | 9 Technology Dr |
| City | West Lebanon |
| State | NH |
| ZIP | 03784 |
| Country | United States |
| Fiscal year | 2025 |
| Inspection end date | Mar 5, 2025 |
| Classification | No Action Indicated (NAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
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