# Apixia Inc – FDA Inspection, Sep 7, 2011

Source: https://www.keypedia.com/records/fda_inspections/apixia-inc/15e2981a-53ed-4306-bf92-9df6188c61b4
Source feed: FDA_Inspections

> FDA inspection 747017 of Apixia Inc, September 07, 2011. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 803. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 747017
- Company Name: Apixia Inc
- Inspection Date: 2011-09-07
- 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: 1

## Related Documents

- [FDA Inspection 1079324 - 2019-02-14](https://www.keypedia.com/records/fda_inspections/apixia-inc/d348da92-f65c-44a1-a67c-bddb03b79b27)
- FDA Inspection 932609 - 2015-06-11

Company: https://www.keypedia.com/companies/apixia-inc/98f467e0-3a1a-4083-ad95-00034e1e587e

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