# FDA Inspection 1187483 - DX PRODUCTS LIMITED - November 03, 2022

Source: https://www.keypedia.com/records/fda_inspections/dx-products-limited/7d904d9d-a336-4e84-8698-106db7cf21ee
Source feed: FDA_Inspections

> FDA Inspection 1187483 for DX PRODUCTS LIMITED on November 03, 2022. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1187483
- Company Name: DX PRODUCTS LIMITED
- Inspection Date: 2022-11-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1187483 - 2022-11-03](https://www.keypedia.com/records/fda_inspections/dx-products-limited/67bb0663-cb4e-4d6f-a2f2-b60092f41a9d)
- [FDA Inspection 1034445 - 2017-12-07](https://www.keypedia.com/records/fda_inspections/dx-products-limited/2c2e7f6a-df5a-4e2a-8ab8-6be4215092d1)
- [FDA Inspection 1034445 - 2017-12-07](https://www.keypedia.com/records/fda_inspections/dx-products-limited/e85a2c6f-f98a-40e5-9d35-3812b2af09bb)

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