FDA Warning Letter — Wyeth Lederle S.R.L

Case 385159 — FEI 3002806766

The FDA took a Warning Letter action against Wyeth Lederle S.R.L on Mar 27, 2013 (Catania, Italy). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action details

Facility
Wyeth Lederle S.R.L
Date
Mar 27, 2013
Fiscal Year
2013
Product Type
Drugs
Center
CDER
Location
Catania (Italy)

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