FDA Warning Letter — Dennis J. Hurwitz, M.D.

Case 397807 — FEI 3010091333

The FDA took a Warning Letter action against Dennis J. Hurwitz, M.D. on September 30, 2013 (Pittsburgh, PA). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Dennis J. Hurwitz, M.D.
Date
September 30, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Pittsburgh, PA (United States)