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FDA Inspection
•Curia New York, Inc.•November 1, 2023

Curia New York, Inc. – FDA Inspection, Nov 1, 2023

Record Details

This FDA Inspection record concerns Curia New York, Inc., with an inspection on November 1, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Curia New York, Inc.
Inspection Date
November 1, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Armen H. Youssoufian (Issuing Officer)
  • Erik W. Koester (FDA Associated Person)
View Company Profile

ID · b92a70af-a048-4448-afdc-07423c595f70

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1221790
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Curia New York, Inc.

7
DateClassificationOfficeProject area
February 5, 2026OAIDrug Quality Assurance
November 9, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 22, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 15, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 30, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Curia New York, Inc.
  • FDA Inspection 1305832 - 2026-02-05
  • FDA Inspection 1035437 - 2017-11-09
  • FDA Inspection 927304 - 2015-05-22
  • FDA Inspection 863460 - 2014-01-15
  • FDA Inspection 816479 - 2013-01-30

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