FDA Inspection 874557 — Wyeth Farma SA

Wyeth Farma SA — FEI 3003973260

The FDA completed an inspection of Wyeth Farma SA on Jan 30, 2014 in San Sebastian De Los Reyes. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Biologics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 30, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
San Sebastian De Los Reyes (Spain)

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