FDA Inspection 1278352 — OsteoMed, LLC

OsteoMed, LLC — FEI 2027754

The FDA completed an inspection of OsteoMed, LLC on August 8, 2025 in Addison, 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
August 8, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Addison, TX (United States)