# FDA Inspection 1060935 - KR Medical Technologies, LLC. - August 03, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/kr-medical-technologies-llc/fdef53d7-a3b7-4cd6-a14f-ab0e07a3f8d1/
Source feed: FDA_Inspections

> FDA Inspection 1060935 for KR Medical Technologies, LLC. on August 03, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1060935
- Company Name: KR Medical Technologies, LLC.
- Inspection Date: 2018-08-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1060935 - 2018-08-03](https://www.globalkeysolutions.net/api/records/fda_inspections/kr-medical-technologies-llc/203ea5cf-b718-4a09-8686-f6c5692ed484/)
- [FDA Inspection 903448 - 2014-11-14](https://www.globalkeysolutions.net/api/records/fda_inspections/kr-medical-technologies-llc/240da379-a89e-4e74-96c9-0bcea22daf59/)
- [FDA Inspection 903448 - 2014-11-14](https://www.globalkeysolutions.net/api/records/fda_inspections/kr-medical-technologies-llc/57dc3af1-262b-4d34-9db4-bd5033db14e9/)

Company: https://www.globalkeysolutions.net/companies/kr-medical-technologies-llc/c87c1fa1-3cd0-40a3-8f2f-f6ddedf3e2e2

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