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FDA Inspection
•Lonza Biologics Plc•March 31, 2017

Lonza Biologics Plc – FDA Inspection, Mar 31, 2017

Record Details

This FDA Inspection record concerns Lonza Biologics Plc, with an inspection on March 31, 2017, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Lonza Biologics Plc
Inspection Date
March 31, 2017
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Maria J. Lopez- Barragan (Issuing Officer)
  • Thuy T. Nguyen (FDA Associated Person)
View Company Profile

ID · 99bf7b21-6489-44e9-8ccb-b34c642e76c3

Inspection Facts

Inspection number
1021064
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Lonza Biologics Plc

5
DateClassificationOfficeProject area
October 13, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 28, 2018Not classifiedOffice of Inspections and Investigations
September 5, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 24, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 24, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Lonza Biologics Plc
  • FDA Inspection 1202907 - 2022-10-13
  • FDA Inspection 1070651 - 2018-09-28
  • FDA Inspection 1097017 - 2018-09-05
  • FDA Inspection 978909 - 2016-06-24
  • FDA Inspection 801062 - 2012-09-24

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