# FDA Inspection 755755 - Ortho Prime Direct Inc - December 12, 2011

Source: https://www.keypedia.com/records/fda_inspections/ortho-prime-direct-inc/2dad4b91-c0f2-46eb-8c5d-ab9986ebcfb6
Source feed: FDA_Inspections

> FDA Inspection 755755 for Ortho Prime Direct Inc on December 12, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 755755
- Company Name: Ortho Prime Direct Inc
- Inspection Date: 2011-12-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 755755 - 2011-12-12](https://www.keypedia.com/records/fda_inspections/ortho-prime-direct-inc/f217db50-ac8e-456b-bed0-6d130d0693e9)

Company: https://www.keypedia.com/companies/ortho-prime-direct-inc/faadefed-d1de-4e1f-93ba-65460b10db8c

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