# FDA Inspection 1050398 - Miele & Cie. KG - April 19, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/miele-cie-kg/db8ffef4-5010-4fc9-b1d7-46d57ff97f8a
Source feed: FDA_Inspections

> FDA Inspection 1050398 for Miele & Cie. KG on April 19, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1050398
- Company Name: Miele & Cie. KG
- Inspection Date: 2018-04-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 970472 - 2016-04-25](https://www.globalkeysolutions.net/records/fda_inspections/miele-cie-kg/fbfd3253-08b9-4dd0-b7ea-62d509ae23f2)

Company: https://www.globalkeysolutions.net/companies/miele-cie-kg/31228504-608e-4d4f-80b6-524416b6f42e

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