# FDA Inspection 992008 - Gureak Navarra - October 20, 2016

Source: https://www.keypedia.com/records/fda_inspections/gureak-navarra/a7725ea1-6b31-410b-ae46-ce87c256bc51
Source feed: FDA_Inspections

> FDA Inspection 992008 for Gureak Navarra on October 20, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 992008
- Company Name: Gureak Navarra
- Inspection Date: 2016-10-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/gureak-navarra/0931cf4d-1543-4281-b6c6-220f74dc8fcc

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