# FDA Inspection 1006991 - Synthes Balsthal - March 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/synthes-balsthal/302967b4-231e-436f-8464-c6ef472ecd0a
Source feed: FDA_Inspections

> FDA Inspection 1006991 for Synthes Balsthal on March 23, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1006991
- Company Name: Synthes Balsthal
- Inspection Date: 2017-03-23
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1006991 - 2017-03-23](https://www.keypedia.com/records/fda_inspections/synthes-balsthal/848636e0-84b0-4fd9-addd-2336d86e69eb)

Company: https://www.keypedia.com/companies/synthes-balsthal/8d5f0ccb-bccc-42e7-be78-d28bc10edd97

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