# eCordum, Inc. – FDA Inspection, Jul 12, 2023

Source: https://www.keypedia.com/records/fda_inspections/ecordum-inc/ae0b9e91-52ef-4131-a7f7-d74013a86c53
Source feed: FDA_Inspections

> FDA inspection 1210291 of eCordum, Inc., July 12, 2023. Classification: Voluntary Action Indicated (VAI). 17 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1210291
- Company Name: eCordum, Inc.
- Inspection Date: 2023-07-12
- 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: 17

## Related Officers

- [Company Rep](https://www.keypedia.com/people/kwong-p-lee/f4778925-1fad-4988-9e39-86482896c4fa)

Company: https://www.keypedia.com/companies/ecordum-inc/55dca54f-9911-4dcd-b7ec-1e811d84c413

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