# FDA Inspection 1123162 - Synergy Health Daniken AG - March 05, 2020

Source: https://www.keypedia.com/records/fda_inspections/synergy-health-daniken-ag/79be1979-be97-4cf6-bb69-742ba6af21f6
Source feed: FDA_Inspections

> FDA Inspection 1123162 for Synergy Health Daniken AG on March 05, 2020. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1123162
- Company Name: Synergy Health Daniken AG
- Inspection Date: 2020-03-05
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1281950 - 2024-01-24](https://www.keypedia.com/records/fda_inspections/synergy-health-daniken-ag/d933296b-67c6-46b9-8c1d-2d85165955d4)
- [FDA Inspection 658610 - 2010-03-03](https://www.keypedia.com/records/fda_inspections/synergy-health-daniken-ag/144738e8-9982-4957-905d-2da0453f6eba)
- [FDA Inspection 658610 - 2010-03-03](https://www.keypedia.com/records/fda_inspections/synergy-health-daniken-ag/89fb19d0-1fdc-4c48-8586-b148721aaf4a)

Company: https://www.keypedia.com/companies/synergy-health-daniken-ag/6ec521b5-5417-469e-80e7-7de432bf3e1a

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