FDA inspection
Coopervision Manufacturing, Ltd.: FDA inspection ending Nov 14, 2002
FDA inspection 251725 · Voluntary Action Indicated (VAI) · Southampton
Key facts
| Inspection ID | 251725 |
|---|---|
| Firm | Coopervision Manufacturing, Ltd. |
| FEI number | 3002806417 |
| Address | Unit 2, Hamble Court Business Park; Hamble Lane |
| City | Southampton |
| Fiscal year | 2003 |
| Inspection end date | Nov 14, 2002 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
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