# Accutron Inc – FDA Inspection, Jul 21, 2010

Source: https://www.keypedia.com/records/fda_inspections/accutron-inc/bed8e2c1-49be-4c1c-95f0-d0ea8bc1d56e
Source feed: FDA_Inspections

> FDA inspection 674490 of Accutron Inc, July 21, 2010. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 806 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 674490
- Company Name: Accutron Inc
- Inspection Date: 2010-07-21
- 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 895787 - 2014-09-12
- [FDA Inspection 756182 - 2011-12-07](https://www.keypedia.com/records/fda_inspections/accutron-inc/88812da9-be6e-46fd-a2fc-81fd6eb15d2f)

Company: https://www.keypedia.com/companies/accutron-inc/33a923f0-b304-497b-b4dc-a3ca1581dc2d

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