FDA Warning Letter — Andropharm, LLC

Case 522784 — FEI 3013364296

The FDA took a Warning Letter action against Andropharm, LLC on Jun 5, 2017 (Boca Raton, FL). The action was issued by CDER and concerns drugs products.

Action Details

Facility
Andropharm, LLC
Date
Jun 5, 2017
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Boca Raton, FL (United States)

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