# SONA NANOTECH · 89-08 · CANADA — FDA import alert red lists: firms subject to detention without physical examination For SONA NANOTECH · 89-08 · CANADA, import alert is 89-08; import alert name is "Detention Without Physical Examination of Devices without Approved PMA's or IDE's and Other Devices Not Substantially Equivalent or Without a 510(k)"; country is CANADA; product is COVID-19 LFA; product code is 83 Q - - KP Coronavirus antigen detection test system; date published is 05/14/2021; address is 2-1 Research Dr , Dartmouth, Nova Scotia CANADA, verified against its source on 2026-09-16. - **Firm:** SONA NANOTECH _(verified: appears in the quote below)_ - **Import alert:** 89-08 - **Import alert name:** "Detention Without Physical Examination of Devices without Approved PMA's or IDE's and Other Devices Not Substantially Equivalent or Without a 510(k)" - **Country:** CANADA _(verified: appears in the quote below)_ - **Address:** 2-1 Research Dr , Dartmouth, Nova Scotia CANADA _(verified: appears in the quote below)_ - **Date published:** 05/14/2021 _(verified: appears in the quote below)_ - **Product code:** 83 Q - - KP Coronavirus antigen detection test system. _(verified: appears in the quote below)_ - **Product:** COVID-19 LFA _(verified: appears in the quote below)_ ## What the source says > SONA NANOTECH Date Published : 05/14/2021 2-1 Research Dr , Dartmouth, Nova Scotia CANADA 83 Q - - KP Coronavirus antigen detection test system. Date Published: 05/14/2021 Desc: COVID-19 LFA ## The same source also states > SONA NANOTECH Date Published : 05/14/2021 2001-1969 Upper Water St , Halifax, Nova Scotia CANADA 83 Q - - KP Coronavirus antigen detection test system. Date Published: 05/14/2021 Desc: COVID-19 LFA Source: https://www.accessdata.fda.gov/cms_ia/importalert_244.html ## Source - https://www.accessdata.fda.gov/cms_ia/importalert_244.html Last verified: 2026-09-16. Review by: 2026-11-15. Part of [FDA import alert red lists: firms subject to detention without physical examination](https://referencesource.org/fda-import-alert-red-list/).