FDA Inspection 1252583 — FloSpine, LLC

FloSpine, LLC — FEI 3011513267

The FDA completed an inspection of FloSpine, LLC on February 7, 2025 in Boca Raton, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 7, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Boca Raton, FL (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
316821 CFR 820.198(a)Complaints
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures