# Avioq, Inc. – FDA Inspection, Jan 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/avioq-inc/4007711b-1cad-496b-9800-175a9760421a
Source feed: FDA_Inspections

> FDA inspection 1002599 of Avioq, Inc., January 13, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1002599
- Company Name: Avioq, Inc.
- Inspection Date: 2017-01-13
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Center: Biologics
- Office Name: Center for Biologics Evaluation and Research
- Citation Count: 0

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- [FDA Inspection 1042251 - 2017-08-17](https://www.keypedia.com/records/fda_inspections/avioq-inc/5512c30c-abc6-4290-88be-18e3140ea5f2)
- FDA Inspection 913372 - 2015-01-27

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/prabhu-p-raju/2c0aaede-fe16-4431-bc21-614d7f18cb32)

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

Office: https://www.keypedia.com/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d
