# Thoratec Switzerland GMBH – FDA Inspection, May 24, 2018

Source: https://www.keypedia.com/records/fda_inspections/thoratec-switzerland-gmbh/bb107c6f-e409-499f-8d99-df893d1224dd
Source feed: FDA_Inspections

> FDA inspection 1055591 of Thoratec Switzerland GMBH, May 24, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1107843 - 2018-11-01](https://www.keypedia.com/records/fda_inspections/thoratec-switzerland-gmbh/5cd9e18a-88f2-48d1-b5b0-2bbc8169ab57)
- FDA Inspection 724788 - 2011-04-21

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jacqueline-s-warner/d001f4ec-db46-4d78-a5dd-efea7ddfb893)

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