# FDA Inspection 1054641 - DiaSource ImmunoAssays, SA - June 07, 2018

Source: https://www.keypedia.com/records/fda_inspections/diasource-immunoassays-sa/82d9cda6-c06a-459f-9714-7d525ba2e1f4
Source feed: FDA_Inspections

> FDA Inspection 1054641 for DiaSource ImmunoAssays, SA on June 07, 2018. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1054641
- Company Name: DiaSource ImmunoAssays, SA
- Inspection Date: 2018-06-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1054641 - 2018-06-07](https://www.keypedia.com/records/fda_inspections/diasource-immunoassays-sa/7e6bfcf6-f441-407f-9a3d-f878fd586390)

Company: https://www.keypedia.com/companies/diasource-immunoassays-sa/50aeb3be-4728-4b7e-b2ff-f57142a22f47

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