# FDA Inspection 557506 - Datamax Corporation - January 22, 2009

Source: https://www.keypedia.com/records/fda_inspections/datamax-corporation/cec9822a-85cf-4bd8-acad-f8ac8c874191
Source feed: FDA_Inspections

> FDA Inspection 557506 for Datamax Corporation on January 22, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 557506
- Company Name: Datamax Corporation
- Inspection Date: 2009-01-22
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/datamax-corporation/41891f34-392d-4c11-b807-ef772b9427da

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