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FDA Inspection 1122850 — Lonza Manufacturing LLC

Lonza Manufacturing LLC — FEI 3032299571

The FDA completed an inspection of Lonza Manufacturing LLC on March 17, 2020 in Vacaville, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 17, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vacaville, CA (United States)

Facility

Other inspections at this facility

  • 1287278 (VAI Mon Sep 29 2025 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