Core Viewpoint - Hendi Pharmaceutical's subsidiary, Wuhan Baike Pharmaceutical Development Co., Ltd., successfully passed an FDA inspection, confirming compliance with quality standards and enhancing its competitiveness in the international market [1] Group 1: FDA Inspection - The FDA inspection took place from March 10 to March 14, 2025, focusing on raw materials such as fludarabine phosphate, milrinone, granisetron, and furosemide [1] - The inspection report from the FDA confirmed the completion of the inspection, indicating that Baike Pharmaceutical met the necessary requirements [1] Group 2: Market Implications - The successful inspection demonstrates the company's commitment to maintaining quality systems that align with FDA standards, which is crucial for expanding into international markets [1] - This achievement is expected to enhance the competitiveness of the company's raw material products in the global market [1]