# FDA Inspection 1000739 - Euro Diagnostica AB - January 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/euro-diagnostica-ab/ba3afce9-7bb2-4e20-9176-09831eab25a2
Source feed: FDA_Inspections

> FDA Inspection 1000739 for Euro Diagnostica AB on January 19, 2017. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000739
- Company Name: Euro Diagnostica AB
- Inspection Date: 2017-01-19
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1055353 - 2018-04-26](https://www.keypedia.com/records/fda_inspections/euro-diagnostica-ab/bd2b4fa2-ad98-4d99-933b-469746ab901a)
- [FDA Inspection 1000739 - 2017-01-19](https://www.keypedia.com/records/fda_inspections/euro-diagnostica-ab/9b12d268-4009-4cf0-a711-ad344718bd68)

Company: https://www.keypedia.com/companies/euro-diagnostica-ab/7d939a93-9dfc-4058-b2bd-f4769c279603

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