# FDA Inspection 595046 - Acteon, Inc. - July 09, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/acteon-inc/de44553b-ad5f-420d-9014-a1e246523a0e
Source feed: FDA_Inspections

> FDA Inspection 595046 for Acteon, Inc. on July 09, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 595046
- Company Name: Acteon, Inc.
- Inspection Date: 2009-07-09
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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