FDA Warning Letter — Cantrell Drug Company

Case 416764 — FEI 3004483441

The FDA took a Warning Letter action against Cantrell Drug Company on Jan 21, 2015 (Little Rock, AR). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Cantrell Drug Company
Date
Jan 21, 2015
Fiscal Year
2015
Product Type
Drugs
Center
CDER
Location
Little Rock, AR (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.