# FDA Inspection 947248 - Alleima Karlsruhe GmbH - November 04, 2015

Source: https://www.keypedia.com/records/fda_inspections/alleima-karlsruhe-gmbh/419d5018-cc96-4849-a3d0-54a3e567fa47
Source feed: FDA_Inspections

> FDA Inspection 947248 for Alleima Karlsruhe GmbH on November 04, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 947248
- Company Name: Alleima Karlsruhe GmbH
- Inspection Date: 2015-11-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/alleima-karlsruhe-gmbh/0ac53226-2f86-4da7-9e5d-5066c4c794d4

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