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FDA Inspection
•Dipharma Francis Srl•April 20, 2018

Dipharma Francis Srl – FDA Inspection, Apr 20, 2018

Record Details

This FDA Inspection record concerns Dipharma Francis Srl, with an inspection on April 20, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Dipharma Francis Srl
Inspection Date
April 20, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • MRA McCulloughJ (Issuing Officer)
View Company Profile

ID · 419b092b-abf5-474a-b479-5ef3d33e06be

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1126904
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Dipharma Francis Srl

4
DateClassificationOfficeProject area
February 25, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 28, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 7, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 20, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Dipharma Francis Srl
  • FDA Inspection 1202251 - 2022-02-25
  • FDA Inspection 1019767 - 2017-04-28
  • FDA Inspection 871282 - 2014-03-07
  • FDA Inspection 705342 - 2010-12-20

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