# Acteon, Inc. – FDA Inspection, Feb 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/acteon-inc/b5c2f273-9cd5-408c-9812-6d5dc84b1f8a
Source feed: FDA_Inspections

> FDA inspection 1002018 of Acteon, Inc., February 23, 2017. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1002018
- Company Name: Acteon, Inc.
- Inspection Date: 2017-02-23
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 905889 - 2014-12-10](https://www.keypedia.com/records/fda_inspections/acteon-inc/7fc0adc6-924b-4c45-ad96-e8574b5ca69b)
- FDA Inspection 756655 - 2011-12-12
- FDA Inspection 595046 - 2009-07-09

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/meredith-l-sheridan/4021bfe4-3d32-44da-8dc2-e85d1807c000)

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