FDA Warning Letter — Triad Rx, Inc

Case 569659 — FEI 3013497126

The FDA took a Warning Letter action against Triad Rx, Inc on Feb 5, 2019 (Daphne, AL). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action details

Facility
Triad Rx, Inc
Date
Feb 5, 2019
Fiscal Year
2019
Product Type
Drugs
Center
CDER
Location
Daphne, AL (United States)

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