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FDA Inspection
•Syntho Pharmaceuticals, Inc.•February 3, 2009

Syntho Pharmaceuticals, Inc. – FDA Inspection, Feb 3, 2009

Record Details

This FDA Inspection record concerns Syntho Pharmaceuticals, Inc., with an inspection on February 3, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Syntho Pharmaceuticals, Inc.
Inspection Date
February 3, 2009
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 263340af-9e5b-4a30-b8c5-03ad2a046304

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
560541
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Syntho Pharmaceuticals, Inc.

9
DateClassificationOfficeProject area
March 1, 2024Not classifiedNew York District OfficeDrug Quality Assurance
September 3, 2019OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 9, 2017OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 26, 2016OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 23, 2013OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 9 other inspections on the company page
Other documents for Syntho Pharmaceuticals, Inc.
  • FDA Inspection 1231554 - 2024-03-01
  • FDA Inspection 1101047 - 2019-09-03
  • FDA Inspection 1003899 - 2017-03-09
  • FDA Inspection 984108 - 2016-08-26
  • FDA Inspection 844933 - 2013-08-23

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