FDA Warning Letter — Riverpoint Medical, LLC

Case 394102 — FEI 3006981798

The FDA took a Warning Letter action against Riverpoint Medical, LLC on May 1, 2013 (Portland, OR). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Riverpoint Medical, LLC
Date
May 1, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Portland, OR (United States)