# FDA Inspection 1023161 - Synthes Hagendorf GmbH - August 03, 2017

Source: https://www.keypedia.com/records/fda_inspections/synthes-hagendorf-gmbh/975b5e1d-aff4-4517-a8ad-92a8b25e8e05
Source feed: FDA_Inspections

> FDA Inspection 1023161 for Synthes Hagendorf GmbH on August 03, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023161
- Company Name: Synthes Hagendorf GmbH
- Inspection Date: 2017-08-03
- 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-hagendorf-gmbh/ab3e7b99-8bfb-456f-b323-463c6efd0713

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