# Avazzia, Inc – FDA Inspection, Aug 30, 2017

Source: https://www.keypedia.com/records/fda_inspections/avazzia-inc/4fa8f75c-c4d1-4abd-a0a5-f8fed8c04a9b
Source feed: FDA_Inspections

> FDA inspection 1023770 of Avazzia, Inc, August 30, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023770
- Company Name: Avazzia, Inc
- Inspection Date: 2017-08-30
- 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: 3

## Related Documents

- FDA Inspection 673136 - 2010-07-13

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/karen-m-cruz-arenas/6c698301-84ca-4ba7-a79c-309721db2f1b)

Company: https://www.keypedia.com/companies/avazzia-inc/7fc3192e-2878-49e8-851a-e8cc52d4fefb

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