Breaking news: Rainy Consulting has once again broken its own record! The customer has passed the FDA certification audit with zero defects in the United States!

Dongguan Aidishi Electromechanical Equipment Co., Ltd. is a professional factory that produces atomizers and obtained FDA 510K registration in the United States in 2013. This is one of the atomizer companies that was approved to enter the United States early among peers, so the company has taken the lead and gained a considerable sales market in the United States, adding a certain advantage to the FDA certification in the United States.

Aidi Shi and Rui Enni Consulting have had a comprehensive cooperation for many years, and CE/ISO 13485/FDA 510K/FDA factory inspections have always been guided by Rui Enni Consulting. We have already passed [sensitive word] FDA factory inspections in 2016, and in the 2019 re inspection, our stable partner still chose us. Under three months of perfect cooperation and professional guidance, a small company of about 50 people should have hardware that meets the level of a first-class enterprise.

During the factory inspection for FDA certification in the United States from July 8th to 11th, 2019, the review was successfully passed with zero defects, and due to the perfect preparation, the audit process was very smooth and ended one day ahead of schedule. This has set a new record for the coaching and consulting work of Ruini Medical Device Management Co., Ltd. in 2019! This outstanding achievement comes from our professional coaching at Ruini Company and the careful preparation of our clients It is worth celebrating warmly

Shenzhen Ruienni Medical Device Management Co., Ltd. will continue to work hard and provide professional counseling and consultation for customers, as well as professional FDA certification services for you!