FDA Inspection 841845 — Baxter R & D Europe

Baxter R & D Europe — FEI 1000359047

The FDA completed an inspection of Baxter R & D Europe on Jun 21, 2013 in Braine-L'Alleud. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jun 21, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Braine-L'Alleud (Belgium)

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