FDA Inspection 1093156 — Lonza Biologics Porrino SL

Lonza Biologics Porrino SL — FEI 3006067169

The FDA completed an inspection of Lonza Biologics Porrino SL on Mar 23, 2018 in O Porrino. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 23, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
O Porrino (Spain)

Additional details

Mutual Recognition Agreement (MRA)

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