# FDA Inspection 971984 - Heartware, Inc. - May 04, 2016

Source: https://www.keypedia.com/records/fda_inspections/heartware-inc/f4f9237f-1877-4ec0-b68a-cbee214fd5af
Source feed: FDA_Inspections

> FDA Inspection 971984 for Heartware, Inc. on May 04, 2016. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 971984
- Company Name: Heartware, Inc.
- Inspection Date: 2016-05-04
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1058645 - 2018-07-12](https://www.keypedia.com/records/fda_inspections/heartware-inc/5104d940-d430-4459-991f-cda75adfd4e0)
- [FDA Inspection 1058645 - 2018-07-12](https://www.keypedia.com/records/fda_inspections/heartware-inc/860f6a54-65dd-485c-94e3-ccbc83531d23)
- [FDA Inspection 971984 - 2016-05-04](https://www.keypedia.com/records/fda_inspections/heartware-inc/3e3d8df9-a973-4af0-aa2f-cdba688fa05e)
- [FDA Inspection 864927 - 2014-01-24](https://www.keypedia.com/records/fda_inspections/heartware-inc/143971ff-b233-4385-bbc8-17b741d4503e)
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Company: https://www.keypedia.com/companies/heartware-inc/fc9e730f-ca60-46ac-9b88-23a426f2dbfe

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