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FDA Inspection
•Olon S.p.A.•May 24, 2019

Olon S.p.A. – FDA Inspection, May 24, 2019

Record Details

This FDA Inspection record concerns Olon S.p.A., with an inspection on May 24, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Olon S.p.A.
Inspection Date
May 24, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • MRA McCulloughJ (Issuing Officer)
View Company Profile

ID · b62d84c5-0537-4bd2-a1ab-25c8cfa5c95c

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1123156
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Olon S.p.A.

6
DateClassificationOfficeProject area
March 28, 2025VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 13, 2019Not classifiedOffice of Inspections and Investigations
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 1101912 - 2019-09-13
  • FDA Inspection 1063574 - 2017-03-03
  • FDA Inspection 980973 - 2016-05-20
  • FDA Inspection 871564 - 2014-02-28

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