# Acteon, Inc. – FDA Inspection, Dec 10, 2014

Source: https://www.keypedia.com/records/fda_inspections/acteon-inc/7fc0adc6-924b-4c45-ad96-e8574b5ca69b
Source feed: FDA_Inspections

> FDA inspection 905889 of Acteon, Inc., December 10, 2014. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 905889
- Company Name: Acteon, Inc.
- Inspection Date: 2014-12-10
- 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: 3

## Related Documents

- [FDA Inspection 1002018 - 2017-02-23](https://www.keypedia.com/records/fda_inspections/acteon-inc/b5c2f273-9cd5-408c-9812-6d5dc84b1f8a)
- FDA Inspection 756655 - 2011-12-12
- FDA Inspection 595046 - 2009-07-09

Company: https://www.keypedia.com/companies/acteon-inc/0f7a9961-3060-4c78-97cc-825d4bb4047b

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