# AccuMED Corp. – FDA Inspection, Jul 20, 2023

Source: https://www.keypedia.com/records/fda_inspections/accumed-corp/ca42a630-fda8-46cd-b6a8-ab62083990d1
Source feed: FDA_Inspections

> FDA inspection 1214917 of AccuMED Corp., July 20, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1214917
- Company Name: AccuMED Corp.
- Inspection Date: 2023-07-20
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1021505 - 2017-05-25
- [FDA Inspection 859554 - 2013-11-14](https://www.keypedia.com/records/fda_inspections/accumed-corp/dd5c0a08-21f1-4a82-9de9-26f51154e332)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/esteban-beltran/9a9bf6b2-ecdf-494c-82f4-5ef5932d629a)

Company: https://www.keypedia.com/companies/accumed-corp/77079d51-2c3d-455a-995c-92c13a78c39a

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