FDA inspection
Teligent Pharma, Inc.: FDA inspection ending Oct 19, 2017
FDA inspection 1032023 · Voluntary Action Indicated (VAI) · Buena, NJ
Key facts
| Inspection ID | 1032023 |
|---|---|
| Firm | Teligent Pharma, Inc. |
| FEI number | 1000526875 |
| Address | 105 Lincoln Avenue |
| City | Buena |
| State | NJ |
| ZIP | 08310 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Oct 19, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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