# DiaSource ImmunoAssays, SA – FDA Inspection, Jun 7, 2018

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

> FDA inspection 1054641 of DiaSource ImmunoAssays, SA, June 07, 2018. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1054641
- Company Name: DiaSource ImmunoAssays, SA
- Inspection Date: 2018-06-07
- 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 Officers

- [FDA Associated Person](https://www.keypedia.com/people/janet-pulver/d46b01cd-8c3d-4a54-bb91-843e0f94de89)

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