FDA Inspection 1063006 — Ardena U.S. LLC

Ardena U.S. LLC — FEI 3003563645

The FDA completed an inspection of Ardena U.S. LLC on July 13, 2018 in Somerset, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 13, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Somerset, NJ (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)