# FDA Inspection 819239 - Avioq, Inc. - February 08, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/avioq-inc/c4b6d351-0217-41e8-a841-98c34422bff2
Source feed: FDA_Inspections

> FDA Inspection 819239 for Avioq, Inc. on February 08, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 819239
- Company Name: Avioq, Inc.
- Inspection Date: 2013-02-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/avioq-inc/7bf5243a-9d4e-4335-bd22-7d4075729928

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