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FDA Inspection
•Apicore Pharmaceuticals Private Ltd•January 25, 2018

Apicore Pharmaceuticals Private Ltd – FDA Inspection, Jan 25, 2018

Record Details

This FDA Inspection record concerns Apicore Pharmaceuticals Private Ltd, with an inspection on January 25, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Apicore Pharmaceuticals Private Ltd
Inspection Date
January 25, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Daveta L. Bailey (Company Rep)
  • Tajah L. Blackburn (FDA Associated Person)
View Company Profile

ID · 74e610b5-5b2f-4768-8711-6f527d200aee

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1040683
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Apicore Pharmaceuticals Private Ltd

5
DateClassificationOfficeProject area
May 5, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 8, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 25, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 13, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 12, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Apicore Pharmaceuticals Private Ltd
  • FDA Inspection 1206636 - 2023-05-05
  • FDA Inspection 1113142 - 2019-11-08
  • FDA Inspection 965189 - 2016-03-25
  • FDA Inspection 885835 - 2014-06-13
  • FDA Inspection 745467 - 2011-09-12

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