Establishment registration
KEELER LTD.
FDA establishment registration 1000391004 · WINDSOR, BERKSHIRE Windsor and Maidenhead, GB
Key facts
| Registration number | 1000391004 |
|---|---|
| Establishment name | KEELER LTD. |
| Owner/operator | KEELER LTD. |
| Owner/operator number | 9011500 |
| FEI number | 1000391004 |
| Address | CLEWER HILL RD. |
| City | WINDSOR, BERKSHIRE Windsor and Maidenhead |
| Country | GB |
| Establishment types | Contract manufacturer, Specification developer |
| Registration valid through | 2026 |
| Product codes listed | EBA, ERA, GEX, HIT, HJH, HJM, HJO, HKI, HKL, HKN, HKX, HKY, HLI, HLJ, HOQ, HPA, HQF, HRN, ITX, IYO, MMQ |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- 1–9 FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database