# FDA Inspection 1008028 - Aesku Group GmbH & Co. KG - March 02, 2017

Source: https://www.keypedia.com/records/fda_inspections/aesku-group-gmbh-co-kg/5f347ea4-a7cf-424f-9000-01d98f0e9707
Source feed: FDA_Inspections

> FDA Inspection 1008028 for Aesku Group GmbH & Co. KG on March 02, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1008028
- Company Name: Aesku Group GmbH & Co. KG
- Inspection Date: 2017-03-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1008028 - 2017-03-02](https://www.keypedia.com/records/fda_inspections/aesku-group-gmbh-co-kg/71e9b782-ad62-4efe-8a8b-ecb07b979329)

Company: https://www.keypedia.com/companies/aesku-group-gmbh-co-kg/b47ca8d5-16b1-4e6f-94ca-b26458167f5d

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