# FDA Inspection 1210373 - KBL GmbH - June 15, 2023

Source: https://www.keypedia.com/records/fda_inspections/kbl-gmbh/3604845d-c42d-4f5d-a7cd-882b953550e9
Source feed: FDA_Inspections

> FDA Inspection 1210373 for KBL GmbH on June 15, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1210373
- Company Name: KBL GmbH
- Inspection Date: 2023-06-15
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1210373 - 2023-06-15](https://www.keypedia.com/records/fda_inspections/kbl-gmbh/0ec982ca-885d-426e-bb6f-1e11f8a7910b)
- [FDA Inspection 1210373 - 2023-06-15](https://www.keypedia.com/records/fda_inspections/kbl-gmbh/ba7207ad-e4fe-4cb0-9289-71b73a5c40be)
- [FDA Inspection 986138 - 2016-09-02](https://www.keypedia.com/records/fda_inspections/kbl-gmbh/5063a165-3cf8-4df3-b9f7-6ba12eb90b61)
- [FDA Inspection 986138 - 2016-09-02](https://www.keypedia.com/records/fda_inspections/kbl-gmbh/ac2cd409-5e47-4954-9def-9175cfbe3bea)

Company: https://www.keypedia.com/companies/kbl-gmbh/d059bee2-d9c9-4415-b58b-28e1cfd2d3bf

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