FDA Inspection
DX PRODUCTS LIMITEDDX PRODUCTS LIMITED – FDA Inspection, Nov 3, 2022
Record Details
This FDA Inspection record concerns DX PRODUCTS LIMITED, with an inspection on November 3, 2022, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- DX PRODUCTS LIMITED
- Inspection Date
- November 3, 2022
- Product Type
- Devices
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ID · 7d904d9d-a336-4e84-8698-106db7cf21ee
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1187483
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.198(b)Review and evaluation for investigation
- 21 CFR 820.70(g)(2)Periodic equipment inspections
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
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Other FDA inspections of DX PRODUCTS LIMITED
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 8, 2026 | Not classified | Office of Inspections and Investigations | |
| December 7, 2017 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for DX PRODUCTS LIMITED
- FDA Inspection 1323204 - 2026-05-08
- FDA Inspection 1034445 - 2017-12-07
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