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FDA Inspection 1287278 — Lonza Manufacturing LLC

Lonza Manufacturing LLC — FEI 3032299571

The FDA completed an inspection of Lonza Manufacturing LLC on September 29, 2025 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 29, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vacaville, CA (United States)

Facility

Other inspections at this facility

  • 1122850 (NAI Tue Mar 17 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 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))
  • 895423 (NAI Fri Sep 19 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 847467 (VAI Fri Sep 06 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources