# Abbott GmbH – FDA Inspection, Sep 23, 2010

Source: https://www.keypedia.com/records/fda_inspections/abbott-gmbh/286cfcab-dfa1-418b-81d5-cbdf67a45b27
Source feed: FDA_Inspections

> FDA inspection 684828 of Abbott GmbH, September 23, 2010. Classification: Voluntary Action Indicated (VAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 684828
- Company Name: Abbott GmbH
- Inspection Date: 2010-09-23
- 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

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- [FDA Inspection 1076420 - 2018-09-07](https://www.keypedia.com/records/fda_inspections/abbott-gmbh/23a95032-ad8d-477f-b24d-0a5126ab27cc)
- FDA Inspection 839385 - 2013-06-13
- FDA Inspection 770439 - 2012-02-09

Company: https://www.keypedia.com/companies/abbott-gmbh/de254c5b-80ef-453c-a21d-da1f38e1100c

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