# FDA Inspection 596268 - Axiom Worldwide,Inc. - July 10, 2009

Source: https://www.keypedia.com/records/fda_inspections/axiom-worldwideinc/495a6bd4-471b-45bc-a89d-d926effbeee2
Source feed: FDA_Inspections

> FDA Inspection 596268 for Axiom Worldwide,Inc. on July 10, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 596268
- Company Name: Axiom Worldwide,Inc.
- Inspection Date: 2009-07-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 792711 - 2012-07-27](https://www.keypedia.com/records/fda_inspections/axiom-worldwideinc/bd92427c-ffa1-437f-8fba-a1f5920d59ce)
- [FDA Inspection 596268 - 2009-07-10](https://www.keypedia.com/records/fda_inspections/axiom-worldwideinc/9a6e8881-6daf-4fba-a11b-118639252cd1)

Company: https://www.keypedia.com/companies/axiom-worldwideinc/ba45a226-e50c-4f92-a5c3-f1ac2993083d

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