FDA inspection
Hikma Injectables USA, Inc.: FDA inspection ending Apr 12, 2000
FDA inspection 20070 · Voluntary Action Indicated (VAI) · Dayton, NJ
Key facts
| Inspection ID | 20070 |
|---|---|
| Firm | Hikma Injectables USA, Inc. |
| FEI number | 2242985 |
| Address | 36 Stults Rd |
| City | Dayton |
| State | NJ |
| ZIP | 08810-1540 |
| Fiscal year | 2000 |
| Inspection end date | Apr 12, 2000 |
| 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
- 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