# Aesku Systems GmbH & Co. KG – FDA Inspection, Apr 19, 2018

Source: https://www.keypedia.com/records/fda_inspections/aesku-systems-gmbh-co-kg/cfa75762-b4fc-4e52-afb2-614fc1964766
Source feed: FDA_Inspections

> FDA inspection 1051217 of Aesku Systems GmbH & Co. KG, April 19, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- [Company Rep](https://www.keypedia.com/people/sarah-a-hassas/4f142d54-fc28-4bd5-82ad-7e6fa443688c)

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