FDA Inspection 968939 - Oximeter Plus, Inc - March 25, 2016

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Record Details

This FDA Inspection record concerns Oximeter Plus, Inc, with an inspection on March 25, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Oximeter Plus, Inc
Inspection Date: March 25, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · e116b39b-2093-4308-9bb2-183b1c991106

Violation Codes3

21 CFR 820.100(a)21 CFR 820.18421 CFR 820.90(a)

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