# Southwest Technologies Inc - Inspection Records

Source: https://www.keypedia.com/companies/southwest-technologies-inc/26d21ba3-a6b9-4e2e-8023-fa1f6e35c416

> Inspection records and compliance data for Southwest Technologies Inc in Kansas City, Missouri. Access full analysis and detailed observations.

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## Details

- Name: Southwest Technologies Inc
- FEI Number: 1929833
- City: Kansas City
- State: Missouri
- Country Name: United States
- Address Line 1: 1746 E Levee St
- Zip Code: 64116

## Related Documents

- [FDA Inspection 1238793 - Southwest Technologies Inc - 2024-05-16](https://www.keypedia.com/records/fda_inspections/southwest-technologies-inc/c0b584eb-a478-4891-88b2-12cf8a6a35f5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 16, 2024
- [FDA Inspection 1238793 - Southwest Technologies Inc - 2024-05-16](https://www.keypedia.com/records/fda_inspections/southwest-technologies-inc/3fe0ad70-a6bf-4382-a3a2-5a22b39fc52c) — classification: No Action Indicated (NAI), source: FDA, date: May 16, 2024
- [FDA Inspection 1158423 - Southwest Technologies Inc - 2021-12-08](https://www.keypedia.com/records/fda_inspections/southwest-technologies-inc/409fe779-d46a-4cc1-94cb-1a7a83bebf04) — classification: No Action Indicated (NAI), source: FDA, date: December 8, 2021
- [FDA Inspection 1158423 - Southwest Technologies Inc - 2021-12-08](https://www.keypedia.com/records/fda_inspections/southwest-technologies-inc/07e795c6-9a2e-4bdf-9fe9-2e6382734e09) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 8, 2021
- [FDA Inspection 1083228 - Southwest Technologies Inc - 2019-03-20](https://www.keypedia.com/records/fda_inspections/southwest-technologies-inc/a8850239-b0a7-47a1-a194-5fc3bda8c295) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 20, 2019
- [FDA Inspection 1083228 - Southwest Technologies Inc - 2019-03-20](https://www.keypedia.com/records/fda_inspections/southwest-technologies-inc/61eb562e-194a-4766-9636-e3dab3486495) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 20, 2019
- [FDA Inspection 1043100 - Southwest Technologies Inc - 2018-03-05](https://www.keypedia.com/records/fda_inspections/southwest-technologies-inc/e3238e5d-7de7-4e40-8e91-1ca1a82823c8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 5, 2018
- [FDA Inspection 1043100 - Southwest Technologies Inc - 2018-03-05](https://www.keypedia.com/records/fda_inspections/southwest-technologies-inc/3b6edaed-039e-41b9-94e8-12bdebd7090a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 5, 2018
- [FDA Inspection 906251 - Southwest Technologies Inc - 2014-12-09](https://www.keypedia.com/records/fda_inspections/southwest-technologies-inc/47033802-7467-4b58-af5e-5aba8b8bbd1b) — classification: No Action Indicated (NAI), source: FDA, date: December 9, 2014
- [FDA Inspection 906251 - Southwest Technologies Inc - 2014-12-09](https://www.keypedia.com/records/fda_inspections/southwest-technologies-inc/14e23034-86d8-41e9-a64e-57dcfac0b9df) — classification: No Action Indicated (NAI), source: FDA, date: December 9, 2014

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