# FDA Inspection 839385 - Abbott GmbH - June 13, 2013

Source: https://www.keypedia.com/records/fda_inspections/abbott-gmbh/7a3645f4-6e74-4cb2-918f-adadd8283ae3
Source feed: FDA_Inspections

> FDA Inspection 839385 for Abbott GmbH on June 13, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 839385
- Company Name: Abbott GmbH
- Inspection Date: 2013-06-13
- 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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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