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FDA Inspection
•Fareva Mirabel•June 8, 2018

Fareva Mirabel – FDA Inspection, Jun 8, 2018

Record Details

This FDA Inspection record concerns Fareva Mirabel, with an inspection on June 8, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Fareva Mirabel
Inspection Date
June 8, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Vilmary Negron Rodriguez (Issuing Officer)
View Company Profile

ID · 31d6d2f5-b29e-421e-b35c-55c6f2b02e95

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1054784
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Fareva Mirabel

5
DateClassificationOfficeProject area
July 22, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 15, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 19, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 22, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 23, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Fareva Mirabel
  • FDA Inspection 1271381 - 2022-07-22
  • FDA Inspection 1124081 - 2019-03-15
  • FDA Inspection 955347 - 2016-01-19
  • FDA Inspection 885746 - 2014-05-22
  • FDA Inspection 732459 - 2011-05-23

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