# KBL GmbH – FDA Inspection, Sep 2, 2016

Source: https://www.keypedia.com/records/fda_inspections/kbl-gmbh/ac2cd409-5e47-4954-9def-9175cfbe3bea
Source feed: FDA_Inspections

> FDA inspection 986138 of KBL GmbH, September 02, 2016. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 986138
- Company Name: KBL GmbH
- Inspection Date: 2016-09-02
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- 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: 0

## Related Documents

- FDA Inspection 1210373 - 2023-06-15
- [FDA Inspection 1090616 - 2019-05-17](https://www.keypedia.com/records/fda_inspections/kbl-gmbh/b4e1b4e2-2cac-4c13-b623-86ad8f11eaa2)

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