FDA Inspection 876072 - Oximeter Plus, Inc - April 23, 2014

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Record Details

This FDA Inspection record concerns Oximeter Plus, Inc, with an inspection on April 23, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company: Oximeter Plus, Inc
Inspection Date: April 23, 2014
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 39a97519-a366-4c95-918a-0dfa19aaa092

Violation Codes2

21 CFR 820.100(a)21 CFR 820.90(a)

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