# DX PRODUCTS LIMITED – FDA Inspection, Dec 7, 2017

Source: https://www.keypedia.com/records/fda_inspections/dx-products-limited/e85a2c6f-f98a-40e5-9d35-3812b2af09bb
Source feed: FDA_Inspections

> FDA inspection 1034445 of DX PRODUCTS LIMITED, December 07, 2017. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1034445
- Company Name: DX PRODUCTS LIMITED
- Inspection Date: 2017-12-07
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 10

## Related Documents

- FDA Inspection 1323204 - 2026-05-08
- [FDA Inspection 1187483 - 2022-11-03](https://www.keypedia.com/records/fda_inspections/dx-products-limited/7d904d9d-a336-4e84-8698-106db7cf21ee)

## Related Officers

- Issuing Officer

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7