# Miele & Cie. KG – FDA Inspection, Apr 19, 2018

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

> FDA inspection 1050398 of Miele & Cie. KG, April 19, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 1010 and 1030. Form 483 issued. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1050398
- Company Name: Miele & Cie. KG
- Inspection Date: 2018-04-19
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

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

## Related Officers

- Issuing Officer
- Issuing Officer

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

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