# FDA Inspection 1079324 - Apixia Inc - February 14, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/apixia-inc/b2531d5a-fa70-4a0d-ad73-fd17edfaf0a0
Source feed: FDA_Inspections

> FDA Inspection 1079324 for Apixia Inc on February 14, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1079324
- Company Name: Apixia Inc
- Inspection Date: 2019-02-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1079324 - 2019-02-14](https://www.globalkeysolutions.net/records/fda_inspections/apixia-inc/d348da92-f65c-44a1-a67c-bddb03b79b27)
- [FDA Inspection 932609 - 2015-06-11](https://www.globalkeysolutions.net/records/fda_inspections/apixia-inc/26930667-64d6-4bb1-859b-7c7be7553f2c)
- [FDA Inspection 932609 - 2015-06-11](https://www.globalkeysolutions.net/records/fda_inspections/apixia-inc/6b3b9130-72ec-456c-bd74-1ec154a6441d)
- [FDA Inspection 747017 - 2011-09-07](https://www.globalkeysolutions.net/records/fda_inspections/apixia-inc/15e2981a-53ed-4306-bf92-9df6188c61b4)

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

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