FDA Warning Letter — Aztex Enterprises Ltd.

Case 538947 — FEI 3003516782

The FDA took a Warning Letter action against Aztex Enterprises Ltd. on Oct 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
Oct 23, 2017
Fiscal Year
2018
Product Type
Drugs
Center
CDER
Location
Burlington (Canada)

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