FDA Inspection 649103 — Orthofix U.S. LLC
The FDA completed an inspection of Orthofix U.S. LLC on February 23, 2010 in Lewisville, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- February 23, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Lewisville, TX (United States)