# Gureak Navarra – FDA Inspection, Oct 20, 2016

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

> FDA inspection 992008 of Gureak Navarra, October 20, 2016. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- [Company Rep](https://www.keypedia.com/people/roy-baby/69a18ef5-167c-41eb-a57e-3d138a0820c2)

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