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FDA Inspection
•Hefei Lifeon Pharmaceutical Co., Ltd. (API branch)•July 6, 2018

Hefei Lifeon Pharmaceutical Co., Ltd. (API branch) – FDA Inspection, Jul 6, 2018

Record Details

This FDA Inspection record concerns Hefei Lifeon Pharmaceutical Co., Ltd. (API branch), with an inspection on July 6, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Hefei Lifeon Pharmaceutical Co., Ltd. (API branch)
Inspection Date
July 6, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Helen Verdel (FDA Associated Person)
View Company Profile

ID · 57cbd588-fa11-4e9a-9f85-fbcc102c5134

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1065528
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Hefei Lifeon Pharmaceutical Co., Ltd. (API branch)

1
DateClassificationOfficeProject area
November 22, 2024Not classifiedOffice of Inspections and Investigations
Other documents for Hefei Lifeon Pharmaceutical Co., Ltd. (API branch)
  • FDA Inspection 1257894 - 2024-11-22

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