FDA Inspection 1076442 — Janssen Biologics B.V.

Janssen Biologics B.V. — FEI 3002806632

The FDA completed an inspection of Janssen Biologics B.V. on Jun 15, 2018 in Leiden. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jun 15, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Leiden (Netherlands)

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