FDA Inspection 635785 — Tricol Biomedical, Inc.

Tricol Biomedical, Inc. — FEI 3004050854

The FDA completed an inspection of Tricol Biomedical, Inc. on December 2, 2009 in Portland, OR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 2, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Portland, OR (United States)

Additional Details

Sponsor, Contract Research Organization

Citations

IDCFRDescription
292821 CFR 812.40Sponsors' general responsibilities