FDA inspection
JALTEK SYSTEMS LIMITED: FDA inspection ending Jan 26, 2017
FDA inspection 1002621 · No Action Indicated (NAI) · Luton
Key facts
| Inspection ID | 1002621 |
|---|---|
| Firm | JALTEK SYSTEMS LIMITED |
| FEI number | 3007673896 |
| Address | Unit 13, Dencora Way; Sundon Park |
| City | Luton |
| Country | United Kingdom |
| Fiscal year | 2017 |
| Inspection end date | Jan 26, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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