# FDA Inspection 909450 - Ottobock SE & Co. KGaA Formerly Known As Otto Bock Healthcare GmbH - November 27, 2014

Source: https://www.keypedia.com/records/fda_inspections/ottobock-se-co-kgaa-formerly-known-as-otto-bock-healthcare-gmbh/9c3a3bbc-02d0-4d7d-9a51-283a36da0ad6
Source feed: FDA_Inspections

> FDA Inspection 909450 for Ottobock SE & Co. KGaA Formerly Known As Otto Bock Healthcare GmbH on November 27, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 909450
- Company Name: Ottobock SE & Co. KGaA Formerly Known As Otto Bock Healthcare GmbH
- Inspection Date: 2014-11-27
- 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 909450 - 2014-11-27](https://www.keypedia.com/records/fda_inspections/ottobock-se-co-kgaa-formerly-known-as-otto-bock-healthcare-gmbh/a4c1ec88-cbca-4d21-82c7-b82cb4ad5a66)

Company: https://www.keypedia.com/companies/ottobock-se-co-kgaa-formerly-known-as-otto-bock-healthcare-gmbh/6c61fa4c-059c-4bde-9ccb-92d9258762e6

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