FDA Inspection 1032496 — Wyeth Farma SA

Wyeth Farma SA — FEI 3003973260

The FDA completed an inspection of Wyeth Farma SA on Oct 3, 2017 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
Oct 3, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Sebastian De Los Reyes (Spain)

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