# Argon Medical Devices, Inc - Inspection Records

Source: https://www.keypedia.com/companies/argon-medical-devices-inc/faa6d7fb-142e-4639-b975-d5c78e376daa

> Inspection records and compliance data for Argon Medical Devices, Inc in Athens, Texas. Access full analysis and detailed observations.

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## Details

- Name: Argon Medical Devices, Inc
- FEI Number: 1625425
- City: Athens
- State: Texas
- Country Name: United States
- Address Line 1: 1445 Flat Creek Rd
- Zip Code: 75751

## Related Documents

- [483 - Argon Medical Devices, Inc - 2024-03-19](https://www.keypedia.com/records/483/argon-medical-devices-inc/e4cda975-dafe-4b80-b7dd-af68268ce589) — source: FDA, date: March 19, 2024
- [FDA Inspection 1231193 - Argon Medical Devices, Inc - 2024-03-19](https://www.keypedia.com/records/fda_inspections/argon-medical-devices-inc/11b2cc4d-0d87-4658-ab93-3d57fdaaacca) — source: FDA, date: March 19, 2024
- [FDA Inspection 1231193 - Argon Medical Devices, Inc - 2024-03-19](https://www.keypedia.com/records/fda_inspections/argon-medical-devices-inc/9b2b94cf-e78e-48f3-ba7d-ce764b59c431) — source: FDA, date: March 19, 2024
- [FDA Inspection 1159221 - Argon Medical Devices, Inc - 2021-11-04](https://www.keypedia.com/records/fda_inspections/argon-medical-devices-inc/44450798-f7b1-486e-acaf-f4f00d019b52) — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2021
- [FDA Inspection 1159221 - Argon Medical Devices, Inc - 2021-11-04](https://www.keypedia.com/records/fda_inspections/argon-medical-devices-inc/d68d7d5b-64e2-409c-9cef-4e77f13b6e88) — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2021
- [FDA Inspection 975182 - Argon Medical Devices, Inc - 2016-05-27](https://www.keypedia.com/records/fda_inspections/argon-medical-devices-inc/18b65c31-088f-46e4-b15c-0110cc14cd38) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 27, 2016
- [FDA Inspection 975182 - Argon Medical Devices, Inc - 2016-05-27](https://www.keypedia.com/records/fda_inspections/argon-medical-devices-inc/cdf65856-470f-49bb-bcc8-73289400d677) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 27, 2016
- [FDA Inspection 858950 - Argon Medical Devices, Inc - 2013-12-13](https://www.keypedia.com/records/fda_inspections/argon-medical-devices-inc/d6d3f7fa-bb01-481a-9c01-8b63337e2068) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 13, 2013
- [FDA Inspection 858950 - Argon Medical Devices, Inc - 2013-12-13](https://www.keypedia.com/records/fda_inspections/argon-medical-devices-inc/2db26f51-8812-4d01-b90b-b1f773f72053) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 13, 2013
- [FDA Inspection 727486 - Argon Medical Devices, Inc - 2011-05-18](https://www.keypedia.com/records/fda_inspections/argon-medical-devices-inc/e0804e15-5ce5-4bdb-baaa-017a440b8715) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 18, 2011
- [FDA Inspection 727486 - Argon Medical Devices, Inc - 2011-05-18](https://www.keypedia.com/records/fda_inspections/argon-medical-devices-inc/338bf020-b5b3-49a4-a5d5-2ae8522efd4f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 18, 2011

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