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FDA Inspection
•Changzhou SynTheAll Pharmaceutical Co., Ltd•July 19, 2019

Changzhou SynTheAll Pharmaceutical Co., Ltd – FDA Inspection, Jul 19, 2019

Record Details

This FDA Inspection record concerns Changzhou SynTheAll Pharmaceutical Co., Ltd, with an inspection on July 19, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Changzhou SynTheAll Pharmaceutical Co., Ltd
Inspection Date
July 19, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Laurimer Kuilan-Torres (Issuing Officer)
View Company Profile

ID · da6efc96-fe9a-47b0-a501-a82c9d8f1bb6

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1100357
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Changzhou SynTheAll Pharmaceutical Co., Ltd

2
DateClassificationOfficeProject area
March 7, 2025NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 4, 2018Not classifiedOffice of Inspections and Investigations
Other documents for Changzhou SynTheAll Pharmaceutical Co., Ltd
  • FDA Inspection 1262040 - 2025-03-07
  • FDA Inspection 1054750 - 2018-05-04

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