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FDA Inspection
•Xiamen LP Pharmaceutical Co., Ltd.•November 16, 2018

Xiamen LP Pharmaceutical Co., Ltd. – FDA Inspection, Nov 16, 2018

Record Details

This FDA Inspection record concerns Xiamen LP Pharmaceutical Co., Ltd., with an inspection on November 16, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Xiamen LP Pharmaceutical Co., Ltd.
Inspection Date
November 16, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Jonathan W. Chapman (Company Rep)
View Company Profile

ID · d185c543-5c1d-4278-a21e-0f17a0b003e5

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1072549
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Xiamen LP Pharmaceutical Co., Ltd.

3
DateClassificationOfficeProject area
February 28, 2025Not classifiedOffice of Inspections and Investigations
April 19, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 24, 2017Not classifiedOffice of Inspections and Investigations
Other documents for Xiamen LP Pharmaceutical Co., Ltd.
  • FDA Inspection 1266509 - 2025-02-28
  • FDA Inspection 1239875 - 2024-04-19
  • FDA Inspection 1009616 - 2017-03-24

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