# FDA Inspection 932504 - Axiom Medical Inc - June 23, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/axiom-medical-inc/dde442a5-b148-40f8-93ee-60951087f339
Source feed: FDA_Inspections

> FDA Inspection 932504 for Axiom Medical Inc on June 23, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 932504
- Company Name: Axiom Medical Inc
- Inspection Date: 2015-06-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 810325 - 2012-11-19](https://www.globalkeysolutions.net/records/fda_inspections/axiom-medical-inc/ee07ace8-7cff-4333-a714-e2e555a50e4d)
- [FDA Inspection 810325 - 2012-11-19](https://www.globalkeysolutions.net/records/fda_inspections/axiom-medical-inc/a74e5413-4d4f-4b10-998a-65cca43a8921)
- [FDA Inspection 565030 - 2009-01-15](https://www.globalkeysolutions.net/records/fda_inspections/axiom-medical-inc/233911ff-05fe-4b61-9a6e-b44e4df88c14)
- [FDA Inspection 565030 - 2009-01-15](https://www.globalkeysolutions.net/records/fda_inspections/axiom-medical-inc/64ff962a-8b3c-49a7-b7a5-fdb7cb5665b0)

Company: https://www.globalkeysolutions.net/companies/axiom-medical-inc/1aed4e94-de5c-4b29-b8f5-1a0a7ba59e98

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