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FDA Inspection
•Teh Seng Pharmaceutical Mfg. Co., Ltd. 3rd Plant•August 4, 2023

Teh Seng Pharmaceutical Mfg. Co., Ltd. 3rd Plant – FDA Inspection, Aug 4, 2023

Record Details

This FDA Inspection record concerns Teh Seng Pharmaceutical Mfg. Co., Ltd. 3rd Plant, with an inspection on August 4, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Teh Seng Pharmaceutical Mfg. Co., Ltd. 3rd Plant
Inspection Date
August 4, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Bryan A. Galvez (FDA Associated Person)
View Company Profile

ID · f7d00ca4-3f33-42e2-9ac9-43f8f883cb20

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1217407
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Teh Seng Pharmaceutical Mfg. Co., Ltd. 3rd Plant

4
DateClassificationOfficeProject area
September 11, 2026Not classifiedOffice of Inspections and Investigations
September 22, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 29, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 14, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Teh Seng Pharmaceutical Mfg. Co., Ltd. 3rd Plant
  • FDA Inspection 1341316 - 2026-09-11
  • FDA Inspection 1030280 - 2017-09-22
  • FDA Inspection 933844 - 2015-05-29
  • FDA Inspection 824850 - 2013-03-14

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