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FDA Inspection
•Oximeter Plus, Inc•February 20, 2020

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 · c58a080e-283a-46b0-9ad0-64e1e5b31ba9

Violation Codes2
21 CFR 820.50(a)21 CFR 820.90(a)

Full citation text and observation details available on the Dashboard.

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