FDA Inspection 1100338 - Abaxis Inc - August 22, 2019

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Record Details

This FDA Inspection record concerns Abaxis Inc, with an inspection on August 22, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Abaxis Inc
Inspection Date: August 22, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 0d69cb29-42b1-43dc-92c7-38d9a228ea21

Violation Codes3

21 CFR 803.50(a)(1)21 CFR 820.198(d)21 CFR 820.20(c)

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