# FDA Inspection 999726 - Synthes Raron - December 13, 2016

Source: https://www.keypedia.com/records/fda_inspections/synthes-raron/e7f95aa0-ee2a-40f3-a713-77cf6319dbde
Source feed: FDA_Inspections

> FDA Inspection 999726 for Synthes Raron on December 13, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 999726
- Company Name: Synthes Raron
- Inspection Date: 2016-12-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/synthes-raron/d82f180b-b487-49d1-b061-cc59639734bb

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