# FDA Inspection 1200226 - Orthofix U.S. LLC - March 17, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/orthofix-us-llc/fd45fa5e-95e6-4ef1-8b0f-57ddbfd70097/
Source feed: FDA_Inspections

> FDA Inspection 1200226 for Orthofix U.S. LLC on March 17, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1200226
- Company Name: Orthofix U.S. LLC
- Inspection Date: 2023-03-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/orthofix-us-llc/9fbfeb62-83aa-4916-835e-271a38d56ba9

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