FDA Inspection 1093156 — Lonza Biologics Porrino SL

Lonza Biologics Porrino SL — FEI 3006067169

The FDA completed an inspection of Lonza Biologics Porrino SL on March 23, 2018 in O Porrino. 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 23, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
O Porrino (Spain)

Additional Details

Mutual Recognition Agreement (MRA)