FDA Inspection 1195728 - Embolx, Inc. - January 19, 2023

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Record Details

This FDA Inspection record concerns Embolx, Inc., with an inspection on January 19, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company: Embolx, Inc.
Inspection Date: January 19, 2023
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 5e4a7d3e-694a-457f-a9a4-c48bdb574203

Violation Codes6

21 CFR 803.17(a)(1)21 CFR 820.100(b)21 CFR 820.198(e)21 CFR 820.20(b)(3)(i)21 CFR 820.2221 CFR 820.50(a)(1)

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