# Abiomed, Inc. – FDA Inspection, Apr 13, 2023

Source: https://www.keypedia.com/records/fda_inspections/abiomed-inc/fcd3c682-3568-4f99-b9fd-b1b85a1ab600
Source feed: FDA_Inspections

> FDA inspection 1202491 of Abiomed, Inc., April 13, 2023. Classification: Official Action Indicated (OAI). 12 citations under 21 CFR parts 803, 806 and 820. Form 483 issued. 8 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1202491
- Company Name: Abiomed, Inc.
- Inspection Date: 2023-04-13
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 12

## Related Documents

- [FDA Inspection 1234317 - 2025-08-05](https://www.keypedia.com/records/fda_inspections/abiomed-inc/398d847d-0cad-45aa-a294-fe023d6384fe)
- FDA Inspection 1131459 - 2020-10-06
- FDA Inspection 1021587 - 2017-07-27
- FDA Inspection 964416 - 2016-03-25
- FDA Inspection 899479 - 2014-10-09

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/justine-m-corson/5f6e4477-f060-47f1-9165-a63fd6a36226)
- Kalkidan A. Molla

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