# FDA Inspection 940226 - Reha Technology Ag - August 12, 2015

Source: https://www.keypedia.com/records/fda_inspections/reha-technology-ag/55fd38b0-ae57-4481-b815-464b0c0afd08
Source feed: FDA_Inspections

> FDA Inspection 940226 for Reha Technology Ag on August 12, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 940226
- Company Name: Reha Technology Ag
- Inspection Date: 2015-08-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 940226 - 2015-08-12](https://www.keypedia.com/records/fda_inspections/reha-technology-ag/e660300b-6f38-479b-b51e-bc82eff8ba7f)

Company: https://www.keypedia.com/companies/reha-technology-ag/b12d7f06-7404-4c0a-866a-b8b07ddd34a4

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