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FDA Inspection
•RFX Pharmaceutical Co., Ltd.•July 21, 2017

RFX Pharmaceutical Co., Ltd. – FDA Inspection, Jul 21, 2017

Record Details

This FDA Inspection record concerns RFX Pharmaceutical Co., Ltd., with an inspection on July 21, 2017, issued by the Office of Inspections and Investigations, covering human drugs.

Company
RFX Pharmaceutical Co., Ltd.
Inspection Date
July 21, 2017
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Larry K. Hampton (Company Rep)
View Company Profile

ID · abe10b24-3da0-464a-b3b0-0f8ec8b5feb6

Inspection Facts

Inspection number
1023084
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of RFX Pharmaceutical Co., Ltd.

1
DateClassificationOfficeProject area
April 15, 2016VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
Other documents for RFX Pharmaceutical Co., Ltd.
  • FDA Inspection 966362 - 2016-04-15

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