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FDA Inspection
•Huatai Biopharm Inc.•September 19, 2025

Huatai Biopharm Inc. – FDA Inspection, Sep 19, 2025

Record Details

This FDA Inspection record concerns Huatai Biopharm Inc., with an inspection on September 19, 2025, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Huatai Biopharm Inc.
Inspection Date
September 19, 2025
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Matthew B. Casale (FDA Associated Person)
View Company Profile

ID · 4563f6c5-ee00-420e-b42f-5b2b4cc3bd67

Inspection Facts

Inspection number
1288714
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Huatai Biopharm Inc.

4
DateClassificationOfficeProject area
May 23, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 17, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 24, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 10, 2009VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Huatai Biopharm Inc.
  • FDA Inspection 1144990 - 2019-05-23
  • FDA Inspection 979665 - 2016-06-17
  • FDA Inspection 879315 - 2014-04-24
  • FDA Inspection 617852 - 2009-09-10

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