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FDA Inspection
•Curia Italy S.r.l.•May 18, 2018

Curia Italy S.r.l. – FDA Inspection, May 18, 2018

Record Details

This FDA Inspection record concerns Curia Italy S.r.l., with an inspection on May 18, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Curia Italy S.r.l.
Inspection Date
May 18, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Linda F. Murphy (FDA Associated Person)
View Company Profile

ID · 1e154b2b-45c7-47fd-8208-3b961a1f62c0

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1053480
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Curia Italy S.r.l.

4
DateClassificationOfficeProject area
November 17, 2022NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 17, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 28, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 13, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Curia Italy S.r.l.
  • FDA Inspection 1193861 - 2022-11-17
  • FDA Inspection 1123114 - 2019-05-17
  • FDA Inspection 876697 - 2014-03-28
  • FDA Inspection 666161 - 2010-05-13

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