# FDA Inspection 953618 - MAQUET GMBH - November 19, 2015

Source: https://www.keypedia.com/records/fda_inspections/maquet-gmbh/2049b1aa-81a8-4bde-a838-bf901d0fa0b3
Source feed: FDA_Inspections

> FDA Inspection 953618 for MAQUET GMBH on November 19, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 953618
- Company Name: MAQUET GMBH
- Inspection Date: 2015-11-19
- 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/maquet-gmbh/174a176a-2d16-42be-9c74-a904bfc4eafc

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