FDA inspection
Hikma Pharmaceuticals USA Inc.: FDA inspection ending Oct 13, 2016
FDA inspection 990058 · No Action Indicated (NAI) · Bedford, OH
Key facts
| Inspection ID | 990058 |
|---|---|
| Firm | Hikma Pharmaceuticals USA Inc. |
| FEI number | 3012279857 |
| Address | 200 Northfield Rd |
| City | Bedford |
| State | OH |
| ZIP | 44146 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Oct 13, 2016 |
| 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