# FDA Inspection 1195261 - AxioMed, LLC. - January 13, 2023

Source: https://www.keypedia.com/records/fda_inspections/axiomed-llc/1d0e2d9f-ba64-4c4f-a0fa-5c58316a436e
Source feed: FDA_Inspections

> FDA Inspection 1195261 for AxioMed, LLC. on January 13, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1195261
- Company Name: AxioMed, LLC.
- Inspection Date: 2023-01-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/axiomed-llc/1a1b4e57-8e84-40c7-835a-8bb14478182b

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