# FDA Inspection 923689 - OrthogenRx Inc, - April 23, 2015

Source: https://www.keypedia.com/records/fda_inspections/orthogenrx-inc/f59266eb-fdec-4b42-9892-e44b1c0c0493
Source feed: FDA_Inspections

> FDA Inspection 923689 for OrthogenRx Inc, on April 23, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 923689
- Company Name: OrthogenRx Inc,
- Inspection Date: 2015-04-23
- 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 991152 - 2016-10-20](https://www.keypedia.com/records/fda_inspections/orthogenrx-inc/6dd62e58-0168-4abf-8a96-0f1edfbc3854)
- [FDA Inspection 923689 - 2015-04-23](https://www.keypedia.com/records/fda_inspections/orthogenrx-inc/0e7cedbc-713d-43fe-a233-fcfb84b68869)

Company: https://www.keypedia.com/companies/orthogenrx-inc/16bc5bfa-0777-418c-939b-fe686fb495f2

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