# FDA Inspection 1009131 - Oscor Inc. - March 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/oscor-inc/ba6db918-1f26-4e68-97b2-05e10c8ce132
Source feed: FDA_Inspections

> FDA Inspection 1009131 for Oscor Inc. on March 23, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1009131
- Company Name: Oscor Inc.
- Inspection Date: 2017-03-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/oscor-inc/a95066bb-6aae-4335-bb5e-92eebcbf2b17

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