FDA Inspection 815376 — Captiva Spine, Inc

Captiva Spine, Inc — FEI 3006082533

The FDA completed an inspection of Captiva Spine, Inc on January 16, 2013 in Tequesta, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 16, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Tequesta, FL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures