FDA Inspection 842841 — RSB Spine LLC

RSB Spine LLC — FEI 3003597504

The FDA completed an inspection of RSB Spine LLC on August 6, 2013 in Wooster, 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
August 6, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Wooster, OH (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
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