# FDA Inspection 581756 - Synthes, Inc. - April 27, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/synthes-inc/7a7a89d7-4ea5-4f5b-ba05-5adf357be5fb
Source feed: FDA_Inspections

> FDA Inspection 581756 for Synthes, Inc. on April 27, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 581756
- Company Name: Synthes, Inc.
- Inspection Date: 2009-04-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/synthes-inc/9d52931c-933d-4c92-bcf8-3d7b3bc2d279

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