# ReliantHeart Inc. – FDA Inspection, Nov 22, 2016

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

> FDA inspection 995475 of ReliantHeart Inc., November 22, 2016. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 884654 - 2014-06-30
- FDA Inspection 666870 - 2010-04-30
- [FDA Inspection 611763 - 2009-08-06](https://www.keypedia.com/records/fda_inspections/reliantheart-inc/26fe0fa5-b894-44b9-85da-f572b0a84f52)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/ellen-j-tave/a70cd3ed-957f-471b-82ff-24ca7c65bc10)

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