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FDA Inspection
•Nanjing White Whale Pharmaceutical Co., Ltd.•July 21, 2017

Nanjing White Whale Pharmaceutical Co., Ltd. – FDA Inspection, Jul 21, 2017

Record Details

This FDA Inspection record concerns Nanjing White Whale Pharmaceutical Co., Ltd., with an inspection on July 21, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Nanjing White Whale Pharmaceutical Co., Ltd.
Inspection Date
July 21, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Christopher S. Keating
View Company Profile

ID · 701350ce-be1f-40fa-9bd5-fc4b3e9e5672

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1020941
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Nanjing White Whale Pharmaceutical Co., Ltd.

3
DateClassificationOfficeProject area
January 25, 2024Not classifiedOffice of Inspections and Investigations
September 19, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 10, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Nanjing White Whale Pharmaceutical Co., Ltd.
  • FDA Inspection 1228562 - 2024-01-25
  • FDA Inspection 898126 - 2014-09-19
  • FDA Inspection 728992 - 2011-06-10

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