# FDA Inspection 816129 - SenTec AG - October 25, 2012

Source: https://www.keypedia.com/records/fda_inspections/sentec-ag/c2987a4c-813a-495e-adf7-fd571a033d64
Source feed: FDA_Inspections

> FDA Inspection 816129 for SenTec AG on October 25, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 816129
- Company Name: SenTec AG
- Inspection Date: 2012-10-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 816129 - 2012-10-25](https://www.keypedia.com/records/fda_inspections/sentec-ag/0ab31a5e-c0e0-41f6-b235-93bb355281f4)

Company: https://www.keypedia.com/companies/sentec-ag/7bc04694-ce8e-46a5-a68c-73e709164c35

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