Recently, Abbott and Alere announced that they have agreed to amend the current terms of Abbott’s acquisition of US Airil. According to the revised terms, Abbott will acquire US Airil at a price of US$51 per share for a total amount of approximately $5.3 billion, which is a full 500 million less than Abbott’s initial $5.8 billion bid in 2016.
Related links: Abbott once again announced that it will acquire POCT leading company Alere for $5.3 billion
However, the current US Airline shareholders have not yet approved, and other acquisition conditions including the regulatory authorities (including regulatory approval) have not been met. If the above conditions are met, the transaction is expected to be at the end of the third quarter of 2017. Completion, according to the revised terms, the regulatory approval date for the acquisition is extended from April 30, 2017 to September 30, 2017. In addition, the two parties will meet in the Delaware court next week to hold a hearing on the Abbott lawsuit.
Review: the fate of the United States and the United States
On January 30, 2016, Abbott signed an agreement to acquire the global POCT overlord US Airil for $5.8 billion. US Airil also played a pivotal role in the Chinese IVD market, which triggered a shock in the industry.
However, shortly after the announcement of this transaction, the United States has begun to "save luck":
In February, US Airil delayed the submission of its 2015 financial report to securities institutions due to its income problems in China and Africa.
In March, US Airil received a subpoena from the US court to investigate its marketing activities in Africa, Asia and Latin America. The court suspected that US Airil had illegal transactions with agents and health care system officials in these areas.
On July 1, the US court again sent US Airil to investigate its medical insurance bills at Texas Laboratories and possible commercial bribery.
In the same month (July), according to FDA requirements, US Airil recalled the INRatio coagulation analyzer again. The device has been widely used before, but was found to give a wrong monitoring result.
In August, the United States finally announced the 2015 financial data, the three pillars of the product line revenues all declined, and admitted that due to internal management loopholes, need to re-offer the 2013-2015 financial data.
In November, the federal government cancelled the registration of Medicare claims for important US affiliates.
In just 10 months, the United States has suffered a series of problems that hinder business development, including financial omissions, court subpoenas, bribery investigations, medical insurance fraud suspects, product recalls, etc...
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