# FDA Inspection 1051217 - Aesku Systems GmbH & Co. KG - April 19, 2018

Source: https://www.keypedia.com/records/fda_inspections/aesku-systems-gmbh-co-kg/28e8fdd0-ce2a-4ad7-82e0-5b2d435af7a8
Source feed: FDA_Inspections

> FDA Inspection 1051217 for Aesku Systems GmbH & Co. KG on April 19, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1051217
- Company Name: Aesku Systems GmbH & Co. KG
- Inspection Date: 2018-04-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1051217 - 2018-04-19](https://www.keypedia.com/records/fda_inspections/aesku-systems-gmbh-co-kg/cfa75762-b4fc-4e52-afb2-614fc1964766)

Company: https://www.keypedia.com/companies/aesku-systems-gmbh-co-kg/294877b0-cbd5-4836-a174-a8585c205598

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