# FDA Inspection 631146 - B. Braun Avitum AG - November 19, 2009

Source: https://www.keypedia.com/records/fda_inspections/b-braun-avitum-ag/a570e972-4fa3-4a6c-85e1-ea9f830d50be
Source feed: FDA_Inspections

> FDA Inspection 631146 for B. Braun Avitum AG on November 19, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 631146
- Company Name: B. Braun Avitum AG
- Inspection Date: 2009-11-19
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 749548 - 2011-09-29](https://www.keypedia.com/records/fda_inspections/b-braun-avitum-ag/26af4b82-57c8-44ac-835a-277f748a5e9f)
- [FDA Inspection 631146 - 2009-11-19](https://www.keypedia.com/records/fda_inspections/b-braun-avitum-ag/4c0f8419-5492-409a-afb4-41ea4d636e9d)

Company: https://www.keypedia.com/companies/b-braun-avitum-ag/2e613c88-79da-4856-a06f-db0772c55613

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