FDA Inspection 1092778 — Janssen - Cilag Spa.

Janssen - Cilag Spa. — FEI 3003164454

The FDA completed an inspection of Janssen - Cilag Spa. on May 18, 2018 in Latina. 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
May 18, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Latina (Italy)

Additional Details

Mutual Recognition Agreement (MRA)