# Heartware, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/heartware-inc/fc9e730f-ca60-46ac-9b88-23a426f2dbfe

> Inspection records and compliance data for Heartware, Inc. in Miami Lakes, Florida. Access full analysis and detailed observations.

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## Details

- Name: Heartware, Inc.
- FEI Number: 3007042319
- City: Miami Lakes
- State: Florida
- Country Name: United States
- Address Line 1: 14400 Nw 60th Ave
- Zip Code: 33014

## Related Documents

- [483 - Heartware, Inc. - 2021-09-30](https://www.globalkeysolutions.net/records/483/heartware-inc/8eccb497-c1b0-47d2-b89f-a87a3abad0a2) — source: FDA, date: September 30, 2021
- [FDA Inspection 1058645 - Heartware, Inc. - 2018-07-12](https://www.globalkeysolutions.net/records/fda_inspections/heartware-inc/5104d940-d430-4459-991f-cda75adfd4e0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 12, 2018
- [FDA Inspection 1058645 - Heartware, Inc. - 2018-07-12](https://www.globalkeysolutions.net/records/fda_inspections/heartware-inc/860f6a54-65dd-485c-94e3-ccbc83531d23) — classification: Official Action Indicated (OAI), source: FDA, date: July 12, 2018
- [483 - Heartware, Inc. - 2016-05-04](https://www.globalkeysolutions.net/records/483/heartware-inc/08c011b3-65b5-47b5-bf2b-8f8b8e8f1f4b) — source: FDA, date: May 4, 2016
- [FDA Inspection 971984 - Heartware, Inc. - 2016-05-04](https://www.globalkeysolutions.net/records/fda_inspections/heartware-inc/f4f9237f-1877-4ec0-b68a-cbee214fd5af) — classification: Official Action Indicated (OAI), source: FDA, date: May 4, 2016
- [FDA Inspection 971984 - Heartware, Inc. - 2016-05-04](https://www.globalkeysolutions.net/records/fda_inspections/heartware-inc/3e3d8df9-a973-4af0-aa2f-cdba688fa05e) — classification: Official Action Indicated (OAI), source: FDA, date: May 4, 2016
- [483 - Heartware, Inc. - 2014-01-24](https://www.globalkeysolutions.net/records/483/heartware-inc/c477e339-7f14-4aaf-bd4c-1515bd0c6e95) — source: FDA, date: January 24, 2014
- [FDA Inspection 864927 - Heartware, Inc. - 2014-01-24](https://www.globalkeysolutions.net/records/fda_inspections/heartware-inc/143971ff-b233-4385-bbc8-17b741d4503e) — classification: Official Action Indicated (OAI), source: FDA, date: January 24, 2014
- [FDA Inspection 864927 - Heartware, Inc. - 2014-01-24](https://www.globalkeysolutions.net/records/fda_inspections/heartware-inc/9d273baf-ee12-46c3-ba5b-dc236607d480) — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2014
- [FDA Inspection 851937 - Heartware, Inc. - 2013-08-30](https://www.globalkeysolutions.net/records/fda_inspections/heartware-inc/a4b38d59-79fc-4ea4-84b7-e63bba4f565f) — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2013
- [FDA Inspection 851937 - Heartware, Inc. - 2013-08-30](https://www.globalkeysolutions.net/records/fda_inspections/heartware-inc/00b7331f-506d-4eb2-a9ca-12214bcfb9ff) — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2013
- [FDA Inspection 738736 - Heartware, Inc. - 2011-07-20](https://www.globalkeysolutions.net/records/fda_inspections/heartware-inc/38518b3b-f77a-48d6-8270-a39972d43f33) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 20, 2011

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