# FDA Inspection 860811 - Veridiam, Inc - December 23, 2013

Source: https://www.keypedia.com/records/fda_inspections/veridiam-inc/a8379a30-bd45-4f59-8f22-5968e215748b
Source feed: FDA_Inspections

> FDA Inspection 860811 for Veridiam, Inc on December 23, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 860811
- Company Name: Veridiam, Inc
- Inspection Date: 2013-12-23
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 860811 - 2013-12-23](https://www.keypedia.com/records/fda_inspections/veridiam-inc/48e2a4ed-1702-474c-ab87-d548294ae472)
- [FDA Inspection 741755 - 2011-08-26](https://www.keypedia.com/records/fda_inspections/veridiam-inc/b29a55ed-6b26-479e-afde-b2f7bf4f1971)
- [FDA Inspection 741755 - 2011-08-26](https://www.keypedia.com/records/fda_inspections/veridiam-inc/07174cdb-8db7-42e7-aaca-7fd2c8da6e59)

Company: https://www.keypedia.com/companies/veridiam-inc/4fbb429a-ddb1-4155-879e-27d72ed3ca74

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