# FDA Inspection 877910 - Synthes Zuchwil - April 03, 2014

Source: https://www.keypedia.com/records/fda_inspections/synthes-zuchwil/024ce63c-7658-474b-b6a8-2e0086707b35
Source feed: FDA_Inspections

> FDA Inspection 877910 for Synthes Zuchwil on April 03, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 877910
- Company Name: Synthes Zuchwil
- Inspection Date: 2014-04-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 999721 - 2016-12-16](https://www.keypedia.com/records/fda_inspections/synthes-zuchwil/cfbc8911-5388-464c-9613-d2e041883f48)
- [FDA Inspection 877910 - 2014-04-03](https://www.keypedia.com/records/fda_inspections/synthes-zuchwil/cc4c968b-8af6-4be5-ba64-61f825763893)

Company: https://www.keypedia.com/companies/synthes-zuchwil/c9587924-2329-41e2-9ddb-8764af362936

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