# Kub Technologies, Inc. – FDA Inspection, Feb 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/kub-technologies-inc/ce77b365-5406-439d-a0d1-33c8e571a9f3
Source feed: FDA_Inspections

> FDA inspection 1002194 of Kub Technologies, Inc., February 23, 2017. Classification: No Action Indicated (NAI). 4 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1002194
- Company Name: Kub Technologies, Inc.
- Inspection Date: 2017-02-23
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

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- [FDA Inspection 635740 - 2009-12-18](https://www.keypedia.com/records/fda_inspections/kub-technologies-inc/8b5d1fe7-0486-4026-9407-4914b7dada48)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/michael-g-mayfield/ec045e12-d940-4f76-a17f-98ba4a8dd5b9)

Company: https://www.keypedia.com/companies/kub-technologies-inc/edfac1e1-827f-42cd-bf94-b2b50239d4ee

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