# FDA Inspection 1055591 - Thoratec Switzerland GMBH - May 24, 2018

Source: https://www.keypedia.com/records/fda_inspections/thoratec-switzerland-gmbh/3cfe4ea5-5fa1-400a-99e0-2761481fb027
Source feed: FDA_Inspections

> FDA Inspection 1055591 for Thoratec Switzerland GMBH on May 24, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1055591
- Company Name: Thoratec Switzerland GMBH
- Inspection Date: 2018-05-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1055591 - 2018-05-24](https://www.keypedia.com/records/fda_inspections/thoratec-switzerland-gmbh/93082c85-1291-4989-a07f-2d26969fa9b6)
- [FDA Inspection 724788 - 2011-04-21](https://www.keypedia.com/records/fda_inspections/thoratec-switzerland-gmbh/f812ea6c-cd93-413e-86be-497d39c67e24)

Company: https://www.keypedia.com/companies/thoratec-switzerland-gmbh/cc367c75-a2e6-4d95-ad75-290dca3f3936

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