FDA Inspection
Miele & Cie. KGMiele & Cie. KG – FDA Inspection, Apr 25, 2016
Record Details
This FDA Inspection record concerns Miele & Cie. KG, with an inspection on April 25, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Miele & Cie. KG
- Inspection Date
- April 25, 2016
- Product Type
- Devices
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ID · fbfd3253-08b9-4dd0-b7ea-62d509ae23f2
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 970472
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
FDA Citations
1- 21 CFR 1030.10(c)(3)(i)tests--errors and uncertainties accounted for
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Other FDA inspections of Miele & Cie. KG
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 19, 2018 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
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