FDA warning letter · Drugs

Hubei Gedian Humanwell Pharmaceutical Co., Ltd.

Issued · Posted by FDA

Selected passages from the FDA letter

Quoted FDA text from the published dataset. These selected excerpts are not the complete letter.

Passage 1

Failure to clean equipment and utensils to prevent contamination or carry-over of a material that would alter the quality of the API beyond the official or other established specifications.

Passage 2

Failure of your quality unit to exercise its responsibility to ensure the API manufactured at your facility are in compliance with CGMP.