FDA Inspection 629671 — Cenorin, LLC

Cenorin, LLC — FEI 3004153171

The FDA completed an inspection of Cenorin, LLC on October 26, 2009 in Kent, WA. 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
October 26, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Kent, WA (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation
405921 CFR 820.22Quality Audits - defined intervals