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FDA Inspection
•Lilly France S.A.S.•August 28, 2018

Lilly France S.A.S. – FDA Inspection, Aug 28, 2018

Record Details

This FDA Inspection record concerns Lilly France S.A.S., with an inspection on August 28, 2018, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Lilly France S.A.S.
Inspection Date
August 28, 2018
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Wayne E. Seifert (Senior Regulatory Specialist)
View Company Profile

ID · f327e9ea-160b-4d12-8602-054ba10008d1

Inspection Facts

Inspection number
1063854
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Lilly France S.A.S.

8
DateClassificationOfficeProject area
September 29, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 15, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 16, 2020NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 19, 2019VAIOffice of Inspections and InvestigationsNew Drug Evaluation
April 4, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 8 other inspections on the company page
Other documents for Lilly France S.A.S.
  • FDA Inspection 1299456 - 2023-09-29
  • FDA Inspection 1180181 - 2021-01-15
  • FDA Inspection 1117961 - 2020-01-16
  • FDA Inspection 1081382 - 2019-02-19
  • FDA Inspection 1020863 - 2017-04-04

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