# FDA Inspection 807572 - Otto Bock Healthcare Products GmbH - October 19, 2012

Source: https://www.keypedia.com/records/fda_inspections/otto-bock-healthcare-products-gmbh/5a001b3e-8f48-4ccd-8645-3ed25a74a0d2
Source feed: FDA_Inspections

> FDA Inspection 807572 for Otto Bock Healthcare Products GmbH on October 19, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 807572
- Company Name: Otto Bock Healthcare Products GmbH
- Inspection Date: 2012-10-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1110603 - 2019-11-21](https://www.keypedia.com/records/fda_inspections/otto-bock-healthcare-products-gmbh/8ad64522-c2c4-4289-9e52-085e73fb1cab)
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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