FDA Inspection 855852 — Riverpoint Medical, LLC

Riverpoint Medical, LLC — FEI 3006981798

The FDA completed an inspection of Riverpoint Medical, LLC on Dec 2, 2013 in Portland, OR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 2, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Portland, OR (United States)

Citations

IDCFRDescription
311821 CFR 820.75(a)Documentation