# FDA Inspection 891132 - LivaNova USA, Inc. - August 22, 2014

Source: https://www.keypedia.com/records/fda_inspections/livanova-usa-inc/67df494a-d4aa-401e-9a34-5efce8b04950
Source feed: FDA_Inspections

> FDA inspection 891132 of LivaNova USA, Inc., August 22, 2014. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 803. 6 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 891132
- Company Name: LivaNova USA, Inc.
- Inspection Date: 2014-08-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1302110 - 2026-01-16
- FDA Inspection 1261017 - 2025-02-20
- FDA Inspection 1180294 - 2022-08-12
- [FDA Inspection 1141170 - 2021-05-04](https://www.keypedia.com/records/fda_inspections/livanova-usa-inc/e8dc1930-353f-434c-9c25-e8d5506607d1)
- [FDA Inspection 808850 - 2012-12-07](https://www.keypedia.com/records/fda_inspections/livanova-usa-inc/e840ba12-b209-4489-80b4-8681db659f37)

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