FDA Warning Letter — Tedec-Meiji Farma, S.A.

Case 243054 — FEI 3003184440

The FDA took a Warning Letter action against Tedec-Meiji Farma, S.A. on Apr 24, 2012 (Alcala de Henares, Spain). The action was issued by CDER and concerns drugs products. This facility has 4 recent FDA inspections on record.

Action details

Facility
Tedec-Meiji Farma, S.A.
Date
Apr 24, 2012
Fiscal Year
2012
Product Type
Drugs
Center
CDER
Location
Alcala de Henares (Spain)

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