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FDA Inspection
•Orient Pharma Co., Ltd. Yunlin Plant•July 6, 2018

Orient Pharma Co., Ltd. Yunlin Plant – FDA Inspection, Jul 6, 2018

Record Details

This FDA Inspection record concerns Orient Pharma Co., Ltd. Yunlin Plant, with an inspection on July 6, 2018, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Orient Pharma Co., Ltd. Yunlin Plant
Inspection Date
July 6, 2018
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Lindsey S. Fleischman (Company Rep)
View Company Profile

ID · 67b73ca1-769c-4cc8-b767-a5b6b3ce38bb

Inspection Facts

Inspection number
1062312
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Orient Pharma Co., Ltd. Yunlin Plant

4
DateClassificationOfficeProject area
May 23, 2025NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 16, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 3, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 14, 2012NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Orient Pharma Co., Ltd. Yunlin Plant
  • FDA Inspection 1274326 - 2025-05-23
  • FDA Inspection 1077757 - 2018-11-16
  • FDA Inspection 921908 - 2015-04-03
  • FDA Inspection 813081 - 2012-12-14

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