FDA Inspection 1109051 — Baxter SA

Baxter SA — FEI 3005468265

The FDA completed an inspection of Baxter SA on September 27, 2019 in Lessines. 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 27, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lessines (Belgium)