# Robert Bosch Healthcare Systems, Inc. – FDA Inspection, May 22, 2013

Source: https://www.keypedia.com/records/fda_inspections/robert-bosch-healthcare-systems-inc/dc284351-469c-45fc-8b6e-35b5a106a22b
Source feed: FDA_Inspections

> FDA inspection 833686 of Robert Bosch Healthcare Systems, Inc., May 22, 2013. Classification: Voluntary Action Indicated (VAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 833686
- Company Name: Robert Bosch Healthcare Systems, Inc.
- Inspection Date: 2013-05-22
- 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: 0

## Related Documents

- [FDA Inspection 936848 - 2015-07-21](https://www.keypedia.com/records/fda_inspections/robert-bosch-healthcare-systems-inc/7b3f123d-27fe-4d04-ab8d-ff8459129f2e)

Company: https://www.keypedia.com/companies/robert-bosch-healthcare-systems-inc/8848a5d2-6592-490c-9bad-5158453fbf8d

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