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FDA Inspection 893677 — Lonza AG

Lonza AG — FEI 3002930340

The FDA completed an inspection of Lonza AG on August 29, 2014 in Visp. 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
August 29, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Visp (Switzerland)

Facility

Other inspections at this facility

  • 1204183 (VAI Tue Mar 28 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1035618 (VAI Fri Dec 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 967811 (VAI Fri Mar 11 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 877791 (NAI Wed Apr 02 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 826508 (NAI Fri Apr 12 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources