# FDA Inspection 1110603 - Otto Bock Healthcare Products GmbH - November 21, 2019

Source: https://www.keypedia.com/records/fda_inspections/otto-bock-healthcare-products-gmbh/d3413740-944d-4ec8-b65b-ec09b06ed6b0
Source feed: FDA_Inspections

> FDA Inspection 1110603 for Otto Bock Healthcare Products GmbH on November 21, 2019. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1110603
- Company Name: Otto Bock Healthcare Products GmbH
- Inspection Date: 2019-11-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1110603 - 2019-11-21](https://www.keypedia.com/records/fda_inspections/otto-bock-healthcare-products-gmbh/8ad64522-c2c4-4289-9e52-085e73fb1cab)
- [FDA Inspection 807572 - 2012-10-19](https://www.keypedia.com/records/fda_inspections/otto-bock-healthcare-products-gmbh/5a001b3e-8f48-4ccd-8645-3ed25a74a0d2)
- [FDA Inspection 807571 - 2012-10-17](https://www.keypedia.com/records/fda_inspections/otto-bock-healthcare-products-gmbh/a0228759-49d2-4e91-9fda-4f8652686614)

Company: https://www.keypedia.com/companies/otto-bock-healthcare-products-gmbh/105e3de1-6bd3-42cd-bf27-dbc59a6d63a9

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