# FDA Inspection 897171 - Heartsine Technologies Inc - September 16, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/heartsine-technologies-inc/810f5265-c10c-4444-9c27-64e7a220ecbb
Source feed: FDA_Inspections

> FDA Inspection 897171 for Heartsine Technologies Inc on September 16, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 897171
- Company Name: Heartsine Technologies Inc
- Inspection Date: 2014-09-16
- 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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- [FDA Inspection 897171 - 2014-09-16](https://www.globalkeysolutions.net/records/fda_inspections/heartsine-technologies-inc/efc37140-55bc-451d-94da-cb73ad634edb)
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- [FDA Inspection 652945 - 2010-03-16](https://www.globalkeysolutions.net/records/fda_inspections/heartsine-technologies-inc/65c1ef5a-7a4a-4240-9fdd-0a79a89534f7)

Company: https://www.globalkeysolutions.net/companies/heartsine-technologies-inc/be932741-f273-49ae-a309-933fdaa1d098

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