# DX PRODUCTS LIMITED, Wakefield, United Kingdom – FDA Inspections

Source: https://www.keypedia.com/companies/dx-products-limited/6a1dbc10-a328-4a08-8dbf-b4fdaf5ff9e6

> Inspection records and compliance data for DX PRODUCTS LIMITED in Wakefield. 3 FDA inspections on record, 1 Form 483, last inspected May 08, 2026.

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## Details

- Name: DX PRODUCTS LIMITED
- FEI Number: 3010386378
- Address Line 1: Unit 1, Horbury Junction Industrial Estate; Calder Vale Road
- City: Wakefield
- Country Name: United Kingdom
- Address: Unit 1, Horbury Junction Industrial Estate; Calder Vale Road, Wakefield, United Kingdom
- Country: United Kingdom

## Related Documents

- FDA Inspection 1323204 - DX PRODUCTS LIMITED - 2026-05-08 — source: FDA, date: May 8, 2026
- FDA Inspection 1187483 - DX PRODUCTS LIMITED - 2022-11-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 3, 2022
- [FDA Inspection 1187483 - DX PRODUCTS LIMITED - 2022-11-03](https://www.keypedia.com/records/fda_inspections/dx-products-limited/7d904d9d-a336-4e84-8698-106db7cf21ee) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 3, 2022
- FDA Inspection 1034445 - DX PRODUCTS LIMITED - 2017-12-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 7, 2017
- [FDA Inspection 1034445 - DX PRODUCTS LIMITED - 2017-12-07](https://www.keypedia.com/records/fda_inspections/dx-products-limited/e85a2c6f-f98a-40e5-9d35-3812b2af09bb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 7, 2017

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