# KR Medical Technologies, LLC. – FDA Inspection, Aug 3, 2018

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

> FDA inspection 1060935 of KR Medical Technologies, LLC., August 03, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1060935
- Company Name: KR Medical Technologies, LLC.
- Inspection Date: 2018-08-03
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 903448 - 2014-11-14](https://www.keypedia.com/records/fda_inspections/kr-medical-technologies-llc/57dc3af1-262b-4d34-9db4-bd5033db14e9)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/esteban-beltran/9a9bf6b2-ecdf-494c-82f4-5ef5932d629a)

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

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