# FDA Inspection 895787 - Accutron Inc - September 12, 2014

Source: https://www.keypedia.com/records/fda_inspections/accutron-inc/c662161d-e01e-4ac0-9c99-a3a51cf309d9
Source feed: FDA_Inspections

> FDA Inspection 895787 for Accutron Inc on September 12, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 895787
- Company Name: Accutron Inc
- Inspection Date: 2014-09-12
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 895787 - 2014-09-12](https://www.keypedia.com/records/fda_inspections/accutron-inc/0cb96955-1e36-4622-863b-7f6416b441c3)
- [FDA Inspection 756182 - 2011-12-07](https://www.keypedia.com/records/fda_inspections/accutron-inc/88812da9-be6e-46fd-a2fc-81fd6eb15d2f)
- [FDA Inspection 756182 - 2011-12-07](https://www.keypedia.com/records/fda_inspections/accutron-inc/2f6ea65d-0916-4814-b13c-492f3049d617)
- [FDA Inspection 674490 - 2010-07-21](https://www.keypedia.com/records/fda_inspections/accutron-inc/bed8e2c1-49be-4c1c-95f0-d0ea8bc1d56e)
- [FDA Inspection 674490 - 2010-07-21](https://www.keypedia.com/records/fda_inspections/accutron-inc/3e6afbbc-0b6d-4f69-af04-f8ec7ac337b1)

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