FDA Inspection 1014144 — Janssen Alanna L

Janssen Alanna L — FEI 3013532925

The FDA completed an inspection of Janssen Alanna L on May 11, 2017 in San Diego, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 11, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
San Diego, CA (United States)

Additional Details

Clinical Investigator (CI)