FDA inspection
Esteve CDMO US, Inc.: FDA inspection ending Dec 17, 2013
FDA inspection 858655 · No Action Indicated (NAI) · Morton Grove, IL
Key facts
| Inspection ID | 858655 |
|---|---|
| Firm | Esteve CDMO US, Inc. |
| FEI number | 1416120 |
| Address | 8210 Austin Ave |
| City | Morton Grove |
| State | IL |
| ZIP | 60053 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Dec 17, 2013 |
| 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
- 10–99 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