FDA inspection
Dexcel Pharma Technologies - Yokneam Factory: FDA inspection ending Feb 25, 2016
FDA inspection 964374 · No Action Indicated (NAI) · Yokne'Am Ilit
Key facts
| Inspection ID | 964374 |
|---|---|
| Firm | Dexcel Pharma Technologies - Yokneam Factory |
| FEI number | 3008404887 |
| Address | Hi-Tech Park, 10, Ha-Kidma |
| City | Yokne'Am Ilit |
| Country | Israel |
| Fiscal year | 2016 |
| Inspection end date | Feb 25, 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
- No 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