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FDA Inspection 615025 — Lonza Manufacturing LLC

Lonza Manufacturing LLC — FEI 3032299571

The FDA completed an inspection of Lonza Manufacturing LLC on September 28, 2009 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
September 28, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vacaville, CA (United States)

Facility

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  • 1063110 (VAI Wed Aug 22 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 940787 (VAI Fri Aug 28 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources