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FDA Inspection
•Cheng Fong Chemical Co., Ltd. Dayuan Factory•March 9, 2018

Cheng Fong Chemical Co., Ltd. Dayuan Factory – FDA Inspection, Mar 9, 2018

Record Details

This FDA Inspection record concerns Cheng Fong Chemical Co., Ltd. Dayuan Factory, with an inspection on March 9, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Cheng Fong Chemical Co., Ltd. Dayuan Factory
Inspection Date
March 9, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Libia M. Lugo (Issuing Officer)
View Company Profile

ID · 6c2e15bd-11c9-45aa-81e9-dd73178f1b18

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1048388
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Cheng Fong Chemical Co., Ltd. Dayuan Factory

6
DateClassificationOfficeProject area
August 2, 2024VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
August 30, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 14, 2017OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 22, 2016OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 12, 2013VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
View all 6 other inspections on the company page
Other documents for Cheng Fong Chemical Co., Ltd. Dayuan Factory
  • FDA Inspection 1245466 - 2024-08-02
  • FDA Inspection 1102734 - 2019-08-30
  • FDA Inspection 1013194 - 2017-04-14
  • FDA Inspection 969541 - 2016-04-22
  • FDA Inspection 828136 - 2013-04-12

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