FDA Inspection 857616 — Align Spine LLC

Align Spine LLC — FEI 3008770076

The FDA completed an inspection of Align Spine LLC on December 4, 2013 in Crystal Lake, IL. 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
December 4, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Crystal Lake, IL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
63021 CFR 803.17Lack of Written MDR Procedures