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

Source: https://www.keypedia.com/records/fda_inspections/livanova-usa-inc/e840ba12-b209-4489-80b4-8681db659f37
Source feed: FDA_Inspections

> FDA inspection 808850 of LivaNova USA, Inc., December 07, 2012. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR parts 803 and 820. 6 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 10

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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