# FDA Inspection 1020202 - Heartware, Inc. - July 21, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/heartware-inc/4c59db07-42e3-414a-a844-8dc894cc2fa7
Source feed: FDA_Inspections

> FDA Inspection 1020202 for Heartware, Inc. on July 21, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020202
- Company Name: Heartware, Inc.
- Inspection Date: 2017-07-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1020202 - 2017-07-21](https://www.globalkeysolutions.net/records/fda_inspections/heartware-inc/32992e9e-914a-4788-8139-303616685cb2)
- [FDA Inspection 940483 - 2015-07-31](https://www.globalkeysolutions.net/records/fda_inspections/heartware-inc/0a447584-a900-420b-a434-0c9c7acb3fca)

Company: https://www.globalkeysolutions.net/companies/heartware-inc/3737dbe4-524b-4da4-b3bc-8c564221c1d4

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