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FDA Inspection
•Actavis Italy Spa A Socio Unico•May 4, 2018

Actavis Italy Spa A Socio Unico – FDA Inspection, May 4, 2018

Record Details

This FDA Inspection record concerns Actavis Italy Spa A Socio Unico, with an inspection on May 4, 2018, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Actavis Italy Spa A Socio Unico
Inspection Date
May 4, 2018
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Wayne E. Seifert (Senior Regulatory Specialist)
View Company Profile

ID · a2902613-22d2-4313-b81e-bf2090617a9e

Inspection Facts

Inspection number
1050972
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Actavis Italy Spa A Socio Unico

7
DateClassificationOfficeProject area
May 24, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 15, 2019VAICenter for Drug Evaluation and ResearchNew Drug Evaluation
October 17, 2017VAIOffice of Inspections and InvestigationsNew Drug Evaluation
December 6, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 18, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Actavis Italy Spa A Socio Unico
  • FDA Inspection 1119381 - 2019-05-24
  • FDA Inspection 1083251 - 2019-03-15
  • FDA Inspection 1031543 - 2017-10-17
  • FDA Inspection 1010790 - 2016-12-06
  • FDA Inspection 942841 - 2015-09-18

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