# Unetixs Vascular, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/unetixs-vascular-inc/806b7c9a-65a4-49da-9cd3-f6fa05fb9fdd

> Inspection records and compliance data for Unetixs Vascular, Inc. in Warwick, Rhode Island. Access full analysis and detailed observations.

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## Details

- Name: Unetixs Vascular, Inc.
- FEI Number: 1222117
- City: Warwick
- State: Rhode Island
- Country Name: United States
- Address Line 1: 333 Strawberry Field Rd Ste 11
- Zip Code: 02886

## Related Documents

- [WARNING_LETTER - Unetixs Vascular, Inc. - 2025-12-04](https://www.keypedia.com/records/warning_letter/unetixs-vascular-inc/99504038-5005-45ca-b944-b6827dedf8a1) — source: FDA, date: December 4, 2025
- [FDA Inspection 1294258 - Unetixs Vascular, Inc. - 2025-12-04](https://www.keypedia.com/records/fda_inspections/unetixs-vascular-inc/1d7c683e-9172-48b4-91a4-996512d75bc3) — classification: Official Action Indicated (OAI), source: FDA, date: December 4, 2025
- [FDA Inspection 1294258 - Unetixs Vascular, Inc. - 2025-12-04](https://www.keypedia.com/records/fda_inspections/unetixs-vascular-inc/291f4437-011e-4ed5-b280-c4b8c30d3a85) — classification: No Action Indicated (NAI), source: FDA, date: December 4, 2025
- [483 - Unetixs Vascular, Inc. - 2022-09-16](https://www.keypedia.com/records/483/unetixs-vascular-inc/485f00fd-0f64-41db-ae3a-c52fc8f3e20d) — source: FDA, date: September 16, 2022
- [FDA Inspection 1180260 - Unetixs Vascular, Inc. - 2022-09-16](https://www.keypedia.com/records/fda_inspections/unetixs-vascular-inc/21a4b87b-5019-4143-9834-2ebefacb33c3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 16, 2022
- [FDA Inspection 1180260 - Unetixs Vascular, Inc. - 2022-09-16](https://www.keypedia.com/records/fda_inspections/unetixs-vascular-inc/b3e3004a-8475-4d11-986b-876de5b4f385) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 16, 2022
- [483 - Unetixs Vascular, Inc. - 2021-07-30](https://www.keypedia.com/records/483/unetixs-vascular-inc/4f248eff-dec8-4a48-9d48-d2b698f06695) — source: FDA, date: July 30, 2021
- [FDA Inspection 1147542 - Unetixs Vascular, Inc. - 2021-07-30](https://www.keypedia.com/records/fda_inspections/unetixs-vascular-inc/2f918bc7-00ce-49e6-8a73-f5c8f6d223f7) — classification: Official Action Indicated (OAI), source: FDA, date: July 30, 2021
- [FDA Inspection 1147542 - Unetixs Vascular, Inc. - 2021-07-30](https://www.keypedia.com/records/fda_inspections/unetixs-vascular-inc/29d87466-c665-4147-a5e8-5a6fb729ce65) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 30, 2021
- [483 - Unetixs Vascular, Inc. - 2019-10-29](https://www.keypedia.com/records/483/unetixs-vascular-inc/91c017b6-d81d-4303-9612-d2edbc066454) — source: FDA, date: October 29, 2019
- [WARNING_LETTER - Unetixs Vascular, Inc. - 2019-10-29](https://www.keypedia.com/records/warning_letter/unetixs-vascular-inc/a65f7ed2-4a62-4333-a2a8-6226d0a719f8) — source: FDA, date: October 29, 2019
- [FDA Inspection 1107891 - Unetixs Vascular, Inc. - 2019-10-29](https://www.keypedia.com/records/fda_inspections/unetixs-vascular-inc/a4e1eab7-86bf-468f-9dd0-a58f5c614b70) — classification: Official Action Indicated (OAI), source: FDA, date: October 29, 2019
- [FDA Inspection 1107891 - Unetixs Vascular, Inc. - 2019-10-29](https://www.keypedia.com/records/fda_inspections/unetixs-vascular-inc/f63a7f69-64bd-4794-84a1-ec0ab9d058e9) — classification: No Action Indicated (NAI), source: FDA, date: October 29, 2019
- [483 - Unetixs Vascular, Inc. - 2018-06-11](https://www.keypedia.com/records/483/unetixs-vascular-inc/97d4301b-79fe-4c2d-8da4-30eb07529925) — source: FDA, date: June 11, 2018
- [FDA Inspection 1055132 - Unetixs Vascular, Inc. - 2018-06-11](https://www.keypedia.com/records/fda_inspections/unetixs-vascular-inc/d00bd394-db44-4cc7-bba4-68ebf3c94556) — classification: Official Action Indicated (OAI), source: FDA, date: June 11, 2018
- [FDA Inspection 1055132 - Unetixs Vascular, Inc. - 2018-06-11](https://www.keypedia.com/records/fda_inspections/unetixs-vascular-inc/6bd2db89-de9a-4a46-9515-a9980ab230a5) — classification: No Action Indicated (NAI), source: FDA, date: June 11, 2018

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