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FDA Inspection
•Bioindustria Laboratorio Italiano Medicinali S.p.A.•June 21, 2018

Bioindustria Laboratorio Italiano Medicinali S.p.A. – FDA Inspection, Jun 21, 2018

Record Details

This FDA Inspection record concerns Bioindustria Laboratorio Italiano Medicinali S.p.A., with an inspection on June 21, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Bioindustria Laboratorio Italiano Medicinali S.p.A.
Inspection Date
June 21, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Alice S. Tsao (FDA Associated Person)
View Company Profile

ID · cfa2958b-b6b6-46e2-a128-661d1fb48859

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1058986
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Bioindustria Laboratorio Italiano Medicinali S.p.A.

3
DateClassificationOfficeProject area
April 1, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 18, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 7, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Bioindustria Laboratorio Italiano Medicinali S.p.A.
  • FDA Inspection 1209819 - 2022-04-01
  • FDA Inspection 898975 - 2014-09-18
  • FDA Inspection 723865 - 2011-04-07

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