FDA Warning Letter — WellRx LLC

Case 506635 — FEI 3011707930

The FDA took a Warning Letter action against WellRx LLC on September 30, 2016 (Wheaton, IL). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
WellRx LLC
Date
September 30, 2016
Fiscal Year
2016
Product Type
Drugs
Center
CDER
Location
Wheaton, IL (United States)