# FDA Inspection 808850 - LivaNova USA, Inc. - December 07, 2012

Source: https://www.keypedia.com/records/fda_inspections/livanova-usa-inc/629da4c7-74b1-4c67-97ce-4ee0b8575257
Source feed: FDA_Inspections

> FDA Inspection 808850 for LivaNova USA, Inc. on December 07, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 808850
- Company Name: LivaNova USA, Inc.
- Inspection Date: 2012-12-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/livanova-usa-inc/3eed84aa-5d07-449c-a020-ff8b2c23ca35

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