FDA Warning Letter — Zipmed Mesoone

Case 88584 — FEI 3008001974

The FDA took a Warning Letter action against Zipmed Mesoone on Apr 5, 2010 (Fortaleza, Brazil). The action was issued by CDER and concerns drugs products.

Action Details

Facility
Zipmed Mesoone
Date
Apr 5, 2010
Fiscal Year
2010
Product Type
Drugs
Center
CDER
Location
Fortaleza (Brazil)

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