# Sendx Medical Inc, Carlsbad, CA – FDA Inspections

Source: https://www.keypedia.com/companies/sendx-medical-inc/a4b04d63-ec4d-46e1-b7ee-54c51181e126

> Inspection records and compliance data for Sendx Medical Inc in Carlsbad, California. 5 FDA inspections on record, 1 Form 483, last inspected December 04, 2025.

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## Details

- Name: Sendx Medical Inc
- FEI Number: 2027541
- Address Line 1: 1945 Palomar Oaks Way
- City: Carlsbad
- State: California
- Zip Code: 92011
- Country Name: United States
- Address: 1945 Palomar Oaks Way, Carlsbad, California 92011, United States
- Country: United States

## Related Documents

- FDA Inspection 1295680 - Sendx Medical Inc - 2025-12-04 — classification: No Action Indicated (NAI), source: FDA, date: December 4, 2025
- FDA Inspection 1174815 - Sendx Medical Inc - 2022-06-29 — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2022
- FDA Inspection 1174815 - Sendx Medical Inc - 2022-06-29 — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2022
- FDA Inspection 1031157 - Sendx Medical Inc - 2017-10-31 — classification: No Action Indicated (NAI), source: FDA, date: October 31, 2017
- [FDA Inspection 1031157 - Sendx Medical Inc - 2017-10-31](https://www.keypedia.com/records/fda_inspections/sendx-medical-inc/596b746d-d964-478d-bf3c-0a7290ad9c76) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 31, 2017
- FDA Inspection 898205 - Sendx Medical Inc - 2014-09-29 — classification: No Action Indicated (NAI), source: FDA, date: September 29, 2014
- FDA Inspection 898205 - Sendx Medical Inc - 2014-09-29 — classification: No Action Indicated (NAI), source: FDA, date: September 29, 2014
- FDA Inspection 557428 - Sendx Medical Inc - 2009-01-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 20, 2009
- [FDA Inspection 557428 - Sendx Medical Inc - 2009-01-20](https://www.keypedia.com/records/fda_inspections/sendx-medical-inc/df27ac09-afbb-4182-90ea-0c8306fcde67) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 20, 2009

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