# FDA Inspection 995475 - ReliantHeart Inc. - November 22, 2016

Source: https://www.keypedia.com/records/fda_inspections/reliantheart-inc/cd68a2fc-bf50-483c-a9c9-d78c83b5058c
Source feed: FDA_Inspections

> FDA Inspection 995475 for ReliantHeart Inc. on November 22, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 995475
- Company Name: ReliantHeart Inc.
- Inspection Date: 2016-11-22
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 995475 - 2016-11-22](https://www.keypedia.com/records/fda_inspections/reliantheart-inc/50c343d7-2791-4bb3-a0b4-a92e20e1f841)
- [FDA Inspection 884654 - 2014-06-30](https://www.keypedia.com/records/fda_inspections/reliantheart-inc/12a065cf-2418-4ee3-b5fd-0fb33750974b)
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- [FDA Inspection 666870 - 2010-04-30](https://www.keypedia.com/records/fda_inspections/reliantheart-inc/d7305921-7d49-4c79-867e-5d36e302fe99)
- [FDA Inspection 611763 - 2009-08-06](https://www.keypedia.com/records/fda_inspections/reliantheart-inc/26fe0fa5-b894-44b9-85da-f572b0a84f52)

Company: https://www.keypedia.com/companies/reliantheart-inc/23e79cbc-483f-462f-bc1a-6f8a0379e26e

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