FDA Warning Letter — Richard E. Ringel, M.D.

Case 56383 — FEI 3007335984

The FDA took a Warning Letter action against Richard E. Ringel, M.D. on May 20, 2009 (Baltimore, MD). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Richard E. Ringel, M.D.
Date
May 20, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Baltimore, MD (United States)