# FDA Inspection 782375 - OrthoPro LLC - May 16, 2012

Source: https://www.keypedia.com/records/fda_inspections/orthopro-llc/1a0d611e-51b2-4fae-971c-e8145fd0f57e
Source feed: FDA_Inspections

> FDA Inspection 782375 for OrthoPro LLC on May 16, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 782375
- Company Name: OrthoPro LLC
- Inspection Date: 2012-05-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 782375 - 2012-05-16](https://www.keypedia.com/records/fda_inspections/orthopro-llc/4c67172c-2ba1-49bc-a6b2-d51e1078264d)

Company: https://www.keypedia.com/companies/orthopro-llc/b2275841-66e6-4754-9762-0f3cb32c152e

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