# FDA Inspection 1050506 - De Soutter Medical Ltd - April 26, 2018

Source: https://www.keypedia.com/records/fda_inspections/de-soutter-medical-ltd/162610ed-e183-4eba-8a4f-a141fea33616
Source feed: FDA_Inspections

> FDA Inspection 1050506 for De Soutter Medical Ltd on April 26, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1050506
- Company Name: De Soutter Medical Ltd
- Inspection Date: 2018-04-26
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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