# ReliantHeart Inc. – FDA Inspection, Aug 6, 2009

Source: https://www.keypedia.com/records/fda_inspections/reliantheart-inc/26fe0fa5-b894-44b9-85da-f572b0a84f52
Source feed: FDA_Inspections

> FDA inspection 611763 of ReliantHeart Inc., August 06, 2009. Classification: Official Action Indicated (OAI). 2 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 611763
- Company Name: ReliantHeart Inc.
- Inspection Date: 2009-08-06
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 995475 - 2016-11-22](https://www.keypedia.com/records/fda_inspections/reliantheart-inc/cd68a2fc-bf50-483c-a9c9-d78c83b5058c)
- FDA Inspection 884654 - 2014-06-30
- FDA Inspection 666870 - 2010-04-30

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