FDA inspection
G&B Electronic Design Ltd.: FDA inspection ending Nov 23, 2006
FDA inspection 450318 · No Action Indicated (NAI) · Bordon
Key facts
| Inspection ID | 450318 |
|---|---|
| Firm | G&B Electronic Design Ltd. |
| FEI number | 3004213020 |
| Address | 54 Industrial Estate, 56 Woolmer Way |
| City | Bordon |
| Fiscal year | 2007 |
| Inspection end date | Nov 23, 2006 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
| Warning letter | UCM076364 |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- Yes 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