# Heartsine Technologies Inc – FDA Inspection, Aug 4, 2009

Source: https://www.keypedia.com/records/fda_inspections/heartsine-technologies-inc/2bb1f4ea-e9fa-442c-bb0b-d84149b8a141
Source feed: FDA_Inspections

> FDA inspection 601913 of Heartsine Technologies Inc, August 04, 2009. Classification: Official Action Indicated (OAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 601913
- Company Name: Heartsine Technologies Inc
- Inspection Date: 2009-08-04
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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- [FDA Inspection 847671 - 2013-08-22](https://www.keypedia.com/records/fda_inspections/heartsine-technologies-inc/e05d9d50-5d24-4eac-8a93-333c0b7104c2)
- [FDA Inspection 652945 - 2010-03-16](https://www.keypedia.com/records/fda_inspections/heartsine-technologies-inc/d9901874-2565-44f2-a52e-c1022a2d9fb0)

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

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