FDA Inspection 634610 — Tricol Biomedical, Inc.

Tricol Biomedical, Inc. — FEI 3004050854

The FDA completed an inspection of Tricol Biomedical, Inc. on December 11, 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). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 11, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Portland, OR (United States)