FDA Inspection
KBL GmbHKBL GmbH – FDA Inspection, Sep 2, 2016
Record Details
This FDA Inspection record concerns KBL GmbH, with an inspection on September 2, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- KBL GmbH
- Inspection Date
- September 2, 2016
- Product Type
- Devices
View Company Profile
ID · ac2cd409-5e47-4954-9def-9175cfbe3bea
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 986138
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
Other FDA inspections of KBL GmbH
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 15, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 17, 2019 | Not classified | Office of Inspections and Investigations | Radiation Control and Health Safety Act |
Other documents for KBL GmbH
- FDA Inspection 1210373 - 2023-06-15
- FDA Inspection 1090616 - 2019-05-17
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