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FDA Inspection 868667 — OsteoMed, LLC

OsteoMed, LLC — FEI 2027754

The FDA completed an inspection of OsteoMed, LLC on February 28, 2014 in Addison, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 28, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Addison, TX (United States)

Facility

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FDA data resources