FDA Inspection
Heartsine Technologies IncHeartsine Technologies Inc – FDA Inspection, Aug 4, 2009
Record Details
This FDA Inspection record concerns Heartsine Technologies Inc, with an inspection on August 4, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Heartsine Technologies Inc
- Inspection Date
- August 4, 2009
- Product Type
- Devices
View Company Profile
ID · 2bb1f4ea-e9fa-442c-bb0b-d84149b8a141
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 601913
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Heartsine Technologies Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| May 3, 2018 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| September 16, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 22, 2013 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 16, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Heartsine Technologies Inc
- FDA Inspection 1068673 - 2018-05-03
- FDA Inspection 897171 - 2014-09-16
- FDA Inspection 847671 - 2013-08-22
- FDA Inspection 652945 - 2010-03-16
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