# Accutome,  Inc – FDA Inspection, Jul 3, 2018

Source: https://www.keypedia.com/records/fda_inspections/accutome-inc/f0bf7c62-a984-43ec-8223-bcacbe7f14e9
Source feed: FDA_Inspections

> FDA inspection 1057783 of Accutome,  Inc, July 03, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1057783
- Company Name: Accutome,  Inc
- Inspection Date: 2018-07-03
- 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: 0

## Related Documents

- FDA Inspection 894258 - 2014-09-05
- FDA Inspection 575624 - 2009-04-03

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/brian-s-keefer/4fec578b-ca72-4d79-8634-3a9fe7ecd9a5)
- [Company Rep](https://www.keypedia.com/people/daniel-t-lee/8147e5b2-2065-42e3-b86c-36c0231f74cc)

Company: https://www.keypedia.com/companies/accutome-inc/a82d8f4b-1c21-4b93-8f43-7239f857ebe3

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