FDA Inspection 1046499 — Janssen Biotech, Inc.

Janssen Biotech, Inc. — FEI 3001610451

The FDA completed an inspection of Janssen Biotech, Inc. on March 5, 2018 in Malvern, PA. 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
March 5, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Malvern, PA (United States)