# Orthofix Srl – FDA Inspection, Sep 27, 2012

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

> FDA inspection 802729 of Orthofix Srl, September 27, 2012. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

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