# FDA 483 - Euro Diagnostica AB - January 19, 2017

Source: https://www.globalkeysolutions.net/records/483/euro-diagnostica-ab/67be2b88-1daa-46b9-9af8-a9c764fdd2f4

> FDA 483 for Euro Diagnostica AB on January 19, 2017. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Euro Diagnostica AB
- Inspection Date: 2017-01-19
- Product Type: device
- Office Name: Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)

## Related Documents

- [WARNING_LETTER - 2017-01-19](https://www.globalkeysolutions.net/records/warning_letter/euro-diagnostica-ab/97b48702-50cb-453c-a7ce-6c8b00d75341)

## Related Officers

- [Dedicated Device Cadre](https://www.globalkeysolutions.net/people/dedicated-device-cadre/693932db-dd86-453f-9b51-a63444b07281)
- [Consumer Safety Officer](https://www.globalkeysolutions.net/people/catherine-j-laufmann/920b7656-2847-408d-ba15-3989283d8c94)

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

Office: https://www.globalkeysolutions.net/offices/division-of-clinical-evidence-and-analysis-1-clinical-policy-and-quality/5f95da17-30bb-423f-b892-5ea041823fbd