# Abaxis Inc – FDA Inspection, Apr 25, 2018

Source: https://www.keypedia.com/records/fda_inspections/abaxis-inc/b33f676a-8144-4285-9696-d193002e595f
Source feed: FDA_Inspections

> FDA inspection 1049551 of Abaxis Inc, April 25, 2018. Classification: Official Action Indicated (OAI). 3 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1049551
- Company Name: Abaxis Inc
- Inspection Date: 2018-04-25
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3
- Enforcement Type: WARNING_LETTER

## Related Documents

- [FDA Inspection 1100338 - 2019-08-22](https://www.keypedia.com/records/fda_inspections/abaxis-inc/f15efc1c-a332-4496-bf72-54378aaa76ad)
- FDA Inspection 894936 - 2014-09-10
- FDA Inspection 775878 - 2012-04-03
- FDA Inspection 703154 - 2010-12-22

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/ian-a-pilcher/d82e7599-0d0b-4373-902b-ee5868e8bd23)
- Issuing Officer

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