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FDA Inspection
•Changzhou SynTheAll Pharmaceutical Co., Ltd•March 7, 2025

Changzhou SynTheAll Pharmaceutical Co., Ltd – FDA Inspection, Mar 7, 2025

Record Details

This FDA Inspection record concerns Changzhou SynTheAll Pharmaceutical Co., Ltd, with an inspection on March 7, 2025, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Changzhou SynTheAll Pharmaceutical Co., Ltd
Inspection Date
March 7, 2025
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Andrew Le (FDA Associated Person)
  • Angelica M. Hernandez (Issuing Officer)
View Company Profile

ID · 77c3b759-a95d-4362-8d1a-87ac53524a25

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1262040
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Changzhou SynTheAll Pharmaceutical Co., Ltd

2
DateClassificationOfficeProject area
July 19, 2019NAICenter 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 1100357 - 2019-07-19
  • FDA Inspection 1054750 - 2018-05-04

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