FDA inspection
Accugenix LLC: FDA inspection ending Jan 17, 2017
FDA inspection 1007057 · No Action Indicated (NAI) · Newark, DE
Key facts
| Inspection ID | 1007057 |
|---|---|
| Firm | Accugenix LLC |
| FEI number | 3002920000 |
| Address | 614 Interchange Blvd |
| City | Newark |
| State | DE |
| ZIP | 19711 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Jan 17, 2017 |
| 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
- Yes Form FDA 483 issued
- Yes 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