FDA Inspection 1278352 — OsteoMed, LLC

OsteoMed, LLC — FEI 2027754

The FDA completed an inspection of OsteoMed, LLC on Aug 8, 2025 in Addison, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 8, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Addison, TX (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.