# Apixia Inc – FDA Inspection, Feb 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/apixia-inc/d348da92-f65c-44a1-a67c-bddb03b79b27
Source feed: FDA_Inspections

> FDA inspection 1079324 of Apixia Inc, February 14, 2019. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1079324
- Company Name: Apixia Inc
- Inspection Date: 2019-02-14
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 932609 - 2015-06-11
- [FDA Inspection 747017 - 2011-09-07](https://www.keypedia.com/records/fda_inspections/apixia-inc/15e2981a-53ed-4306-bf92-9df6188c61b4)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/kelvin-cheung/ded61aee-4b4b-4049-a67c-19d971475be7)

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