FDA Inspection 989724 — Seratec SAS

Seratec SAS — FEI 3003666337

The FDA completed an inspection of Seratec SAS on September 16, 2016 in Courville Sur Eure. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 16, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Courville Sur Eure (France)