# FDA Inspection 997732 - SentreHeart Inc - December 02, 2016

Source: https://www.keypedia.com/records/fda_inspections/sentreheart-inc/a038ad8d-723d-48b9-bc9b-6bd7078ba4a3
Source feed: FDA_Inspections

> FDA Inspection 997732 for SentreHeart Inc on December 02, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 997732
- Company Name: SentreHeart Inc
- Inspection Date: 2016-12-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 997732 - 2016-12-02](https://www.keypedia.com/records/fda_inspections/sentreheart-inc/2aee08bb-f6cc-4d93-a359-46162c2b8504)
- [FDA Inspection 822093 - 2013-03-19](https://www.keypedia.com/records/fda_inspections/sentreheart-inc/5303dfd6-bf18-4d92-a93b-f81b4d273771)
- [FDA Inspection 822093 - 2013-03-19](https://www.keypedia.com/records/fda_inspections/sentreheart-inc/3f91bf25-23cd-4529-ade4-ed457799ed88)

Company: https://www.keypedia.com/companies/sentreheart-inc/6968994b-6fc7-4db0-ba01-2a866b5058aa

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