# 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 for LivaNova USA, Inc. on August 22, 2014. Classification: Voluntary Action Indicated (VAI).

---

## Details

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

## Related Documents

- [FDA Inspection 1302110 - 2026-01-16](https://www.keypedia.com/records/fda_inspections/livanova-usa-inc/2c7c2c88-aedb-4eca-9f1b-4ecc6da6c591)
- [FDA Inspection 1261017 - 2025-02-20](https://www.keypedia.com/records/fda_inspections/livanova-usa-inc/ac0d6e7e-7901-46af-a847-25b68f68bf55)
- [FDA Inspection 1261017 - 2025-02-20](https://www.keypedia.com/records/fda_inspections/livanova-usa-inc/498f0640-f1c9-4126-a7a1-bb775ef56d0b)
- [FDA Inspection 1180294 - 2022-08-12](https://www.keypedia.com/records/fda_inspections/livanova-usa-inc/9bd4e3a1-94cc-4f23-bbb6-de9d754aa1d6)
- [FDA Inspection 1141170 - 2021-05-04](https://www.keypedia.com/records/fda_inspections/livanova-usa-inc/6d935f08-8174-4dff-8643-b53193c00075)

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
