FDA inspection
Provita Eurotech Ltd.: FDA inspection ending Jun 15, 2016
FDA inspection 976047 · No Action Indicated (NAI) · Omagh
Key facts
| Inspection ID | 976047 |
|---|---|
| Firm | Provita Eurotech Ltd. |
| FEI number | 3003114347 |
| Address | 31 Milltown Road |
| City | Omagh |
| Country | United Kingdom |
| Fiscal year | 2016 |
| Inspection end date | Jun 15, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| Product type | Veterinary |
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