FDA Warning Letter — 2187954 ALBERTA INC.

Case 672166 — FEI 3027888319

The FDA took a Warning Letter action against 2187954 ALBERTA INC. on Apr 30, 2024 (Lethbridge, Canada). The action was issued by CDER and concerns drugs products.

Action Details

Facility
2187954 ALBERTA INC.
Date
Apr 30, 2024
Fiscal Year
2024
Product Type
Drugs
Center
CDER
Location
Lethbridge (Canada)

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