FDA Warning Letter — Medinatura New Mexico, Inc.

Case 716025 — FEI 1626962

The FDA took a Warning Letter action against Medinatura New Mexico, Inc. on Dec 10, 2025 (Albuquerque, NM). The action was issued by CDER and concerns drugs products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Medinatura New Mexico, Inc.
Date
Dec 10, 2025
Fiscal Year
2026
Product Type
Drugs
Center
CDER
Location
Albuquerque, NM (United States)

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