# Aesku Group GmbH & Co. KG – FDA Inspection, Mar 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/aesku-group-gmbh-co-kg/71e9b782-ad62-4efe-8a8b-ecb07b979329
Source feed: FDA_Inspections

> FDA inspection 1008028 of Aesku Group GmbH & Co. KG, March 02, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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

## Related Documents

- [FDA Inspection 1156862 - 2019-03-29](https://www.keypedia.com/records/fda_inspections/aesku-group-gmbh-co-kg/ecb6e68f-45f2-4968-b29a-b59e690e0edf)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/andrew-j-garufi/567f6aaa-f6f2-45a3-9a58-80b33f3ad021)

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