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FDA Inspection
•Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd•August 18, 2023

Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd – FDA Inspection, Aug 18, 2023

Record Details

This FDA Inspection record concerns Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd, with an inspection on August 18, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd
Inspection Date
August 18, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Wayne D. Mcgrath
View Company Profile

ID · 56605c3c-e0e9-4939-8447-0885ce9f48bc

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1217084
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

Other FDA inspections of Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd

6
DateClassificationOfficeProject area
September 18, 2026Not classifiedOffice of Inspections and Investigations
August 23, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 28, 2017Not classifiedOffice of Inspections and Investigations
July 28, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 2, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd
  • FDA Inspection 1341100 - 2026-09-18
  • FDA Inspection 1064409 - 2018-08-23
  • FDA Inspection 1006423 - 2017-02-28
  • FDA Inspection 985170 - 2016-07-28
  • FDA Inspection 880928 - 2014-05-02

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