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FDA Inspection
•Gemini Pharmaceuticals, Inc.•September 7, 2012

Gemini Pharmaceuticals, Inc. – FDA Inspection, Sep 7, 2012

Record Details

This FDA Inspection record concerns Gemini Pharmaceuticals, Inc., with an inspection on September 7, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Gemini Pharmaceuticals, Inc.
Inspection Date
September 7, 2012
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 8ccd38c4-b04f-4a2f-a1ab-040379671397

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
804876
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Gemini Pharmaceuticals, Inc.

9
DateClassificationOfficeProject area
May 15, 2026VAINew York District OfficeFood Composition, Standards, Labeling and Econ
July 26, 2022VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
August 23, 2018NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
February 16, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 30, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 9 other inspections on the company page
Other documents for Gemini Pharmaceuticals, Inc.
  • FDA Inspection 1317530 - 2026-05-15
  • FDA Inspection 1175407 - 2022-07-26
  • FDA Inspection 1064447 - 2018-08-23
  • FDA Inspection 1041525 - 2018-02-16
  • FDA Inspection 936886 - 2015-06-30

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