FDA Inspection 955103 — Wyeth Farma SA

Wyeth Farma SA — FEI 3003973260

The FDA completed an inspection of Wyeth Farma SA on Dec 18, 2015 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: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 18, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
San Sebastian De Los Reyes (Spain)

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