FDA Inspection 1119401 - Oximeter Plus, Inc - February 20, 2020

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Record Details

This FDA Inspection record concerns Oximeter Plus, Inc, with an inspection on February 20, 2020, issued by the Center for Devices and Radiological Health, covering devices.

Company: Oximeter Plus, Inc
Inspection Date: February 20, 2020
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · e9e77684-42fc-461c-b4ce-6cf7515e38f6

Violation Codes2

21 CFR 820.50(a)21 CFR 820.90(a)

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