# Otto Bock Healthcare Products GmbH – FDA Inspection, Nov 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 of Otto Bock Healthcare Products GmbH, November 21, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 6 other FDA inspections on record for this company.

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## 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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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- [FDA Inspection 1014754 - 2017-06-08](https://www.keypedia.com/records/fda_inspections/otto-bock-healthcare-products-gmbh/cf81c385-54a3-41ba-8a1f-64f56c36227b)
- [FDA Inspection 807572 - 2012-10-19](https://www.keypedia.com/records/fda_inspections/otto-bock-healthcare-products-gmbh/5a001b3e-8f48-4ccd-8645-3ed25a74a0d2)

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