# Abiomed, Inc. – FDA Inspection, Mar 17, 2010

Source: https://www.keypedia.com/records/fda_inspections/abiomed-inc/4c131e12-9285-4fe2-8883-33b8a9b7ac00
Source feed: FDA_Inspections

> FDA inspection 652658 of Abiomed, Inc., March 17, 2010. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803, 806 and 820. 8 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 652658
- Company Name: Abiomed, Inc.
- Inspection Date: 2010-03-17
- 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: 3

## Related Documents

- [FDA Inspection 1234317 - 2025-08-05](https://www.keypedia.com/records/fda_inspections/abiomed-inc/398d847d-0cad-45aa-a294-fe023d6384fe)
- [FDA Inspection 1202491 - 2023-04-13](https://www.keypedia.com/records/fda_inspections/abiomed-inc/fcd3c682-3568-4f99-b9fd-b1b85a1ab600)
- FDA Inspection 1131459 - 2020-10-06
- FDA Inspection 1021587 - 2017-07-27
- FDA Inspection 964416 - 2016-03-25

Company: https://www.keypedia.com/companies/abiomed-inc/bf75e76c-c813-4c91-81e2-a86e5707a511

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