# FDA Inspection 851937 - Heartware, Inc. - August 30, 2013

Source: https://www.keypedia.com/records/fda_inspections/heartware-inc/a4b38d59-79fc-4ea4-84b7-e63bba4f565f
Source feed: FDA_Inspections

> FDA Inspection 851937 for Heartware, Inc. on August 30, 2013. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 851937
- Company Name: Heartware, Inc.
- Inspection Date: 2013-08-30
- Classification: No Action Indicated (NAI)
- 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/f4f9237f-1877-4ec0-b68a-cbee214fd5af)
- [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)

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
