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FDA Inspection
•Olon S.p.A.•September 13, 2019

Olon S.p.A. – FDA Inspection, Sep 13, 2019

Record Details

This FDA Inspection record concerns Olon S.p.A., with an inspection on September 13, 2019, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Olon S.p.A.
Inspection Date
September 13, 2019
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Camerson E. Moore (FDA Associated Person)
View Company Profile

ID · 658daaa4-61fb-4783-8332-226d83d226fd

Inspection Facts

Inspection number
1101912
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Olon S.p.A.

6
DateClassificationOfficeProject area
March 28, 2025VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 24, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 3, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 20, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 28, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Olon S.p.A.
  • FDA Inspection 1279925 - 2025-03-28
  • FDA Inspection 1123156 - 2019-05-24
  • FDA Inspection 1063574 - 2017-03-03
  • FDA Inspection 980973 - 2016-05-20
  • FDA Inspection 871564 - 2014-02-28

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