What are the problems that Odai often faces?
Problems often faced by EUROday when assisting enterprises to export products to the European market:
· The product label does not meet the requirements, and the product is detained by the EU customs
· The products were not recorded/registered and detained by the customs, and we were questioned by the FDA
· The manufacturer failed to pass the annual audit/the certificate was invalid, and we were questioned by the FDA without our knowledge
· The manufacturer stopped production and the certificate was revoked. We were questioned by the FOOD and Drug Administration without our knowledge, but the person in charge of the manufacturer lost contact collectively
· The product was complained to the TV station due to adverse events, and the TV station came to us to learn about the situation
· The former British Odai went bankrupt. Within a week after the replacement, odai was targeted and questioned by the British Food and Drug Administration, and the products could not be exported
· The Italian database was falsely registered by agents
· The German Food and Drug Authority does not recognize a product as a medical product, which happens to experience adverse events in another EU country
· The products were sold to Europe by a foreign trade company with unqualified labels. We were questioned and the manufacturer could not track them
· The Competent Food and Drug Administration of Germany informed us half a day in advance to inspect our work
We (Europe will America) the generation of team is always positive in the face of various problems, respectively in the process of working with Chinese, English, German and Chinese producers and European authorities (ministry of health/food and drug administration), notified body, agents, retailers, supermarkets, and even TV media actively communicate and exchange, to assist producers to properly handle the various events.
