# De Soutter Medical Ltd – FDA Inspection, Feb 2, 2023

Source: https://www.keypedia.com/records/fda_inspections/de-soutter-medical-ltd/554c0807-e76c-4233-9093-eb3a4ceac9e0
Source feed: FDA_Inspections

> FDA inspection 1196589 of De Soutter Medical Ltd, February 02, 2023. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1196589
- Company Name: De Soutter Medical Ltd
- Inspection Date: 2023-02-02
- 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: 4

## Related Documents

- [FDA Inspection 1050506 - 2018-04-26](https://www.keypedia.com/records/fda_inspections/de-soutter-medical-ltd/162610ed-e183-4eba-8a4f-a141fea33616)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/juanj-wu/0d3e8970-b524-49f6-a307-079091b3c91d)

Company: https://www.keypedia.com/companies/de-soutter-medical-ltd/1a272dd7-824e-4fc9-b4fa-d3fdf2e65f70

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