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

Source: https://www.keypedia.com/records/fda_inspections/oximeter-plus-inc/39a97519-a366-4c95-918a-0dfa19aaa092
Source feed: FDA_Inspections

> FDA Inspection 876072 for Oximeter Plus, Inc on April 23, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 876072
- Company Name: Oximeter Plus, Inc
- Inspection Date: 2014-04-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/oximeter-plus-inc/c6e206c4-5e68-4175-a92e-74e69a4fca5a

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7