Company
United KingdomDX PRODUCTS LIMITED, Wakefield, United Kingdom – FDA Inspections
Inspection records and compliance data for DX PRODUCTS LIMITED in Wakefield. 3 FDA inspections on record, 1 Form 483, last inspected May 08, 2026.
Company Profile
This profile covers DX PRODUCTS LIMITED based in Wakefield, United Kingdom.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 2
- NAI
- 0
- Unclassified
- 1
- Form 483s
- 1
- Warning letters
- 0
First inspected December 7, 2017. Last inspected May 8, 2026.
Most cited issue areas
- Lack of or inadequate complaint procedures2 inspections
- Review and evaluation for investigation2 inspections
- Design input - documentation1 inspection
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| May 8, 2026 | Not classified | Medical Devices & Rad Health | 1323204 |
| November 3, 2022 | VAI | Medical Devices & Rad Health · Compliance: Devices | 1187483 |
| December 7, 2017 | VAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 1034445 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
DX PRODUCTS LIMITED
FEI Number
3010386378
Address
Unit 1, Horbury Junction Industrial Estate; Calder Vale Road, Wakefield, United Kingdom
Country
United Kingdom
ID: 6a1dbc10-a328-4a08-8dbf-b4fdaf5ff9e6