# FDA Inspection 924722 - Orthogem Ltd - April 10, 2015

Source: https://www.keypedia.com/records/fda_inspections/orthogem-ltd/6db8706e-dcfc-400f-8a74-3e2510199f98
Source feed: FDA_Inspections

> FDA Inspection 924722 for Orthogem Ltd on April 10, 2015. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 924722
- Company Name: Orthogem Ltd
- Inspection Date: 2015-04-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 924722 - 2015-04-10](https://www.keypedia.com/records/fda_inspections/orthogem-ltd/1d612701-da0f-413d-a983-fc65b6e7471b)
- [FDA Inspection 657608 - 2010-04-09](https://www.keypedia.com/records/fda_inspections/orthogem-ltd/6943ca30-306d-4b99-9f91-150ebf4149d6)

Company: https://www.keypedia.com/companies/orthogem-ltd/fc9ab0a3-8a4b-499a-9530-308dd65a320e

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