FDA Warning Letter — Aztex Enterprises Ltd.

Case 538947 — FEI 3003516782

The FDA took a Warning Letter action against Aztex Enterprises Ltd. on October 23, 2017 (Burlington, Canada). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Aztex Enterprises Ltd.
Date
October 23, 2017
Fiscal Year
2018
Product Type
Drugs
Center
CDER
Location
Burlington (Canada)