# Axiom Worldwide,Inc. – FDA Inspection, Jul 10, 2009

Source: https://www.keypedia.com/records/fda_inspections/axiom-worldwideinc/9a6e8881-6daf-4fba-a11b-118639252cd1
Source feed: FDA_Inspections

> FDA inspection 596268 of Axiom Worldwide,Inc., July 10, 2009. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- 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: 5

## Related Documents

- [FDA Inspection 792711 - 2012-07-27](https://www.keypedia.com/records/fda_inspections/axiom-worldwideinc/bd92427c-ffa1-437f-8fba-a1f5920d59ce)

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