FDA Warning Letter — John Caton Jr

Case 205673 — FEI 3008420267

The FDA took a Warning Letter action against John Caton Jr on August 26, 2011 (Springfield, OR). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
John Caton Jr
Date
August 26, 2011
Fiscal Year
2011
Product Type
Drugs
Center
CDER
Location
Springfield, OR (United States)