# FDA Inspection 1098770 - Kobold, LLC - August 02, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/kobold-llc/bb869a2a-efe6-4633-96b2-f00d5136c54f
Source feed: FDA_Inspections

> FDA Inspection 1098770 for Kobold, LLC on August 02, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1098770
- Company Name: Kobold, LLC
- Inspection Date: 2019-08-02
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1098770 - 2019-08-02](https://www.globalkeysolutions.net/records/fda_inspections/kobold-llc/df756b08-8e5b-4368-8f87-afa8a836d831)

Company: https://www.globalkeysolutions.net/companies/kobold-llc/6c791a8f-cf36-4342-9bc8-22ad5ca15669

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