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FDA Inspection
•Chongqing Huapont Shengchem Pharmaceutical Co Ltd•July 19, 2018

Chongqing Huapont Shengchem Pharmaceutical Co Ltd – FDA Inspection, Jul 19, 2018

Record Details

This FDA Inspection record concerns Chongqing Huapont Shengchem Pharmaceutical Co Ltd, with an inspection on July 19, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Chongqing Huapont Shengchem Pharmaceutical Co Ltd
Inspection Date
July 19, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Dennis Cantellops Paite (Issuing Officer)
View Company Profile

ID · eb955bae-9345-46d4-b5e3-afb13447e996

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1063451
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Chongqing Huapont Shengchem Pharmaceutical Co Ltd

3
DateClassificationOfficeProject area
June 21, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 23, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 1, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Chongqing Huapont Shengchem Pharmaceutical Co Ltd
  • FDA Inspection 1244293 - 2024-06-21
  • FDA Inspection 944071 - 2015-09-23
  • FDA Inspection 806744 - 2012-11-01

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