FDA Warning Letter — Howard M. Gross, M.D.

Case 461452 — FEI 3011123156

The FDA took a Warning Letter action against Howard M. Gross, M.D. on June 29, 2015 (Dayton, OH). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Howard M. Gross, M.D.
Date
June 29, 2015
Fiscal Year
2015
Product Type
Drugs
Center
CDER
Location
Dayton, OH (United States)