# VitalDyne, Inc – FDA Inspection, Jun 24, 2014

Source: https://www.keypedia.com/records/fda_inspections/vitaldyne-inc/9c32e548-8e22-401d-98ee-d92654d394da
Source feed: FDA_Inspections

> FDA inspection 899983 of VitalDyne, Inc, June 24, 2014. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

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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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1227529 - 2023-12-21
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- FDA Inspection 726603 - 2011-05-26
- FDA Inspection 551121 - 2008-12-11

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