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FDA Inspection 779189 — Lonza Manufacturing LLC

Lonza Manufacturing LLC — FEI 3032299571

The FDA completed an inspection of Lonza Manufacturing LLC on March 28, 2012 in Vacaville, CA. 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 28, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vacaville, CA (United States)

Facility

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FDA data resources