FDA Inspection 1006041 — OsteoSymbionics LLC

OsteoSymbionics LLC — FEI 3007223102

The FDA completed an inspection of OsteoSymbionics LLC on March 29, 2017 in Cleveland, OH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 29, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Cleveland, OH (United States)

Citations

IDCFRDescription
323621 CFR 820.72(b)Calibration procedures - content
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
369621 CFR 820.100(b)Documentation
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures