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FDA Inspection
•Everlight Chemical Industrial Corporation Kuanyin II Plant•September 11, 2017

Everlight Chemical Industrial Corporation Kuanyin II Plant – FDA Inspection, Sep 11, 2017

Record Details

This FDA Inspection record concerns Everlight Chemical Industrial Corporation Kuanyin II Plant, with an inspection on September 11, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Everlight Chemical Industrial Corporation Kuanyin II Plant
Inspection Date
September 11, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Andrew J. Idzior (FDA Associated Person)
  • Azza Talaat (FDA Associated Person)
View Company Profile

ID · 802fb82b-846e-4f8d-b3fa-cd01d156b375

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1028465
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Everlight Chemical Industrial Corporation Kuanyin II Plant

4
DateClassificationOfficeProject area
September 26, 2025VAIDrug Quality Assurance
October 18, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 10, 2015OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 13, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Everlight Chemical Industrial Corporation Kuanyin II Plant
  • FDA Inspection 1292578 - 2025-09-26
  • FDA Inspection 1110782 - 2019-10-18
  • FDA Inspection 921902 - 2015-04-10
  • FDA Inspection 783699 - 2012-04-13

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