# Synthes, Inc. – FDA Inspection, Oct 19, 2012

Source: https://www.keypedia.com/records/fda_inspections/synthes-inc/8b68eaea-49dd-47ce-8585-f1c82c466d57
Source feed: FDA_Inspections

> FDA inspection 806156 of Synthes, Inc., October 19, 2012. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 5 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 806156
- Company Name: Synthes, Inc.
- Inspection Date: 2012-10-19
- 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: 1

## Related Documents

- [FDA Inspection 859106 - 2013-11-13](https://www.keypedia.com/records/fda_inspections/synthes-inc/7545c960-4b20-4836-a8be-c6c88057354e)
- FDA Inspection 831886 - 2013-05-16
- [FDA Inspection 732622 - 2011-09-15](https://www.keypedia.com/records/fda_inspections/synthes-inc/9da0f22e-5ccb-4993-89dc-0729f89395aa)
- FDA Inspection 620039 - 2009-10-08
- [FDA Inspection 581756 - 2009-04-27](https://www.keypedia.com/records/fda_inspections/synthes-inc/7a7a89d7-4ea5-4f5b-ba05-5adf357be5fb)

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

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