FDA Warning Letter — AM Rx

Case 728275 — FEI 3044021238

The FDA took a Warning Letter action against AM Rx on Jun 9, 2026 (New York, NY). The action was issued by CDER and concerns drugs products.

Action details

Facility
AM Rx
Date
Jun 9, 2026
Fiscal Year
2026
Product Type
Drugs
Center
CDER
Location
New York, NY (United States)

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