# Kub Technologies, Inc. - Inspection Records

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

> Inspection records and compliance data for Kub Technologies, Inc. in Stratford, Connecticut. Access full analysis and detailed observations.

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## Details

- Name: Kub Technologies, Inc.
- FEI Number: 3006051164
- City: Stratford
- State: Connecticut
- Country Name: United States
- Address Line 1: 111 Research Dr
- Zip Code: 06615

## Related Documents

- [FDA Inspection 1234862 - Kub Technologies, Inc. - 2024-12-19](https://www.keypedia.com/records/fda_inspections/kub-technologies-inc/42598821-2472-4c9f-8e58-7761edec2cb9) — source: FDA, date: December 19, 2024
- [FDA Inspection 1234862 - Kub Technologies, Inc. - 2024-12-19](https://www.keypedia.com/records/fda_inspections/kub-technologies-inc/b3d45567-3925-4572-87c9-f8a9f1592ff0) — classification: No Action Indicated (NAI), source: FDA, date: December 19, 2024
- [FDA Inspection 1234862 - Kub Technologies, Inc. - 2024-12-19](https://www.keypedia.com/records/fda_inspections/kub-technologies-inc/2dd4ce61-8131-4c3a-82ea-577e1a8438ba) — classification: No Action Indicated (NAI), source: FDA, date: December 19, 2024
- [FDA Inspection 1234862 - Kub Technologies, Inc. - 2024-12-19](https://www.keypedia.com/records/fda_inspections/kub-technologies-inc/466a7be3-ffc9-4df0-b375-b456325b8360) — classification: No Action Indicated (NAI), source: FDA, date: December 19, 2024
- [FDA Inspection 1097256 - Kub Technologies, Inc. - 2019-07-16](https://www.keypedia.com/records/fda_inspections/kub-technologies-inc/b3b66548-4054-4a04-b28d-7ed1555ddd86) — classification: No Action Indicated (NAI), source: FDA, date: July 16, 2019
- [FDA Inspection 1097256 - Kub Technologies, Inc. - 2019-07-16](https://www.keypedia.com/records/fda_inspections/kub-technologies-inc/960fafb4-2f6a-4641-9484-bbcd3fc881eb) — classification: No Action Indicated (NAI), source: FDA, date: July 16, 2019
- [FDA Inspection 1002194 - Kub Technologies, Inc. - 2017-02-23](https://www.keypedia.com/records/fda_inspections/kub-technologies-inc/813edfbc-5fbc-4d52-8b3c-54b943214ba5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 23, 2017
- [FDA Inspection 1002194 - Kub Technologies, Inc. - 2017-02-23](https://www.keypedia.com/records/fda_inspections/kub-technologies-inc/ce77b365-5406-439d-a0d1-33c8e571a9f3) — classification: No Action Indicated (NAI), source: FDA, date: February 23, 2017
- [FDA Inspection 1002194 - Kub Technologies, Inc. - 2017-02-23](https://www.keypedia.com/records/fda_inspections/kub-technologies-inc/3113aaac-c042-4f82-9f2b-c553623c7295) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 23, 2017
- [FDA Inspection 833233 - Kub Technologies, Inc. - 2013-05-17](https://www.keypedia.com/records/fda_inspections/kub-technologies-inc/384406b2-514e-4470-a8e5-34d51cd21f79) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 17, 2013

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