FDA Warning Letter — Michael E. Ring, MD

Case 378001 — FEI 3009647958

The FDA took a Warning Letter action against Michael E. Ring, MD on January 14, 2013 (Spokane, WA). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Michael E. Ring, MD
Date
January 14, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Spokane, WA (United States)