# FDA Inspection 1100338 - Abaxis Inc - August 22, 2019

Source: https://www.keypedia.com/records/fda_inspections/abaxis-inc/0d69cb29-42b1-43dc-92c7-38d9a228ea21
Source feed: FDA_Inspections

> FDA Inspection 1100338 for Abaxis Inc on August 22, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100338
- Company Name: Abaxis Inc
- Inspection Date: 2019-08-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1100338 - 2019-08-22](https://www.keypedia.com/records/fda_inspections/abaxis-inc/f15efc1c-a332-4496-bf72-54378aaa76ad)
- [FDA Inspection 1049551 - 2018-04-25](https://www.keypedia.com/records/fda_inspections/abaxis-inc/b33f676a-8144-4285-9696-d193002e595f)
- [FDA Inspection 1049551 - 2018-04-25](https://www.keypedia.com/records/fda_inspections/abaxis-inc/e41c6829-d3a0-46dc-8db9-0a58182c59d6)
- [FDA Inspection 894936 - 2014-09-10](https://www.keypedia.com/records/fda_inspections/abaxis-inc/33a6fd15-68ac-4be4-8d37-fbc16defc085)
- [FDA Inspection 894936 - 2014-09-10](https://www.keypedia.com/records/fda_inspections/abaxis-inc/4af7b6a5-a092-4b69-a73c-f74ccef8046b)

Company: https://www.keypedia.com/companies/abaxis-inc/98392f88-354f-4be2-b781-a75f289470a2

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