# Southwest Technologies Inc – FDA Inspection, Mar 20, 2019

Source: https://www.keypedia.com/records/fda_inspections/southwest-technologies-inc/a8850239-b0a7-47a1-a194-5fc3bda8c295
Source feed: FDA_Inspections

> FDA inspection 1083228 of Southwest Technologies Inc, March 20, 2019. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1083228
- Company Name: Southwest Technologies Inc
- Inspection Date: 2019-03-20
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 1238793 - 2024-05-16](https://www.keypedia.com/records/fda_inspections/southwest-technologies-inc/c0b584eb-a478-4891-88b2-12cf8a6a35f5)
- FDA Inspection 1158423 - 2021-12-08
- [FDA Inspection 1043100 - 2018-03-05](https://www.keypedia.com/records/fda_inspections/southwest-technologies-inc/e3238e5d-7de7-4e40-8e91-1ca1a82823c8)
- FDA Inspection 906251 - 2014-12-09
- FDA Inspection 660612 - 2010-05-04

## Related Officers

- [Investigator](https://www.keypedia.com/people/eric-c-fox/218af117-1551-476f-80ba-172e2cd6baee)

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
