# FDA Inspection 802729 - Orthofix Srl - September 27, 2012

Source: https://www.keypedia.com/records/fda_inspections/orthofix-srl/5f983a07-e9bf-4baa-ab74-eab4f844857b
Source feed: FDA_Inspections

> FDA Inspection 802729 for Orthofix Srl on September 27, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 802729
- Company Name: Orthofix Srl
- Inspection Date: 2012-09-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 802729 - 2012-09-27](https://www.keypedia.com/records/fda_inspections/orthofix-srl/5089820b-5b05-4d96-bc4d-b76d5ada1558)

Company: https://www.keypedia.com/companies/orthofix-srl/1bd0baef-7009-42cd-9228-89ec98228ef9

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