# FDA Inspection 899983 - VitalDyne, Inc - June 24, 2014

Source: https://www.keypedia.com/records/fda_inspections/vitaldyne-inc/756dc6f1-0be6-480f-84d5-6cd2be9a8943
Source feed: FDA_Inspections

> FDA Inspection 899983 for VitalDyne, Inc on June 24, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 899983
- Company Name: VitalDyne, Inc
- Inspection Date: 2014-06-24
- Classification: No Action Indicated (NAI)
- 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/vitaldyne-inc/20c46b19-67ee-43cc-9cde-5a35b0f8cece

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