Department of Defense Statement on People’s Liberation Army Navy Lasing of U.S. Navy P-8A in Unsafe, Unprofessional Manner

Secretary Esper raised concern over an incident on February 17 in which a U.S. Navy P-8A Poseidon maritime patrol aircraft was lased by PRC navy destroyer 161 while flying in airspace above international waters approximately 380 miles west of Guam.


On March 3, 2020, Secretary of Defense Mark T. Esper spoke with the People’s Republic of China (PRC) Minister of National Defense General Wei Fenghe.

During the call, Secretary Esper raised concern over an incident on February 17 in which a U.S. Navy P-8A Poseidon maritime patrol aircraft was lased by PRC navy destroyer 161 while flying in airspace above international waters approximately 380 miles west of Guam.

Secretary Esper called on the People’s Liberation Army to conduct itself safely and professionally in accordance with bilateral agreements and international standards of safety at sea.

The incident underscores the need for the two militaries to enhance bilateral crisis communication mechanisms to ensure incidents like this do not escalate or lead to miscalculation.

The P-8A was operating in international airspace in accordance with international rules and regulations. The PRC navy destroyer’s actions were unsafe and unprofessional.

Additionally, these acts violate the Code for Unplanned Encounters at Sea (CUES), a multilateral agreement reached at the 2014 Western Pacific Naval Symposium to reduce the chance of an incident at sea. CUES specifically addresses the use of lasers that could cause harm to personnel or damage to equipment. The destroyer’s actions were also inconsistent with a Memorandum of Understanding (MOU) between U.S. Department of Defense and the Ministry of National Defense of the PRC regarding rules of behavior for safety of air and maritime encounters.

The laser, which was not visible to the naked eye, was captured by a sensor onboard the P-8A. Weapons-grade lasers could potentially cause serious harm to aircrew and mariners, as well as ship and aircraft systems.

The P-8A is assigned to VP-45, based out of Jacksonville, Florida, and is forward-deployed to Kadena Air Force Base in Okinawa, Japan. The squadron conducts routine operations, maritime patrol and reconnaissance in the U.S. 7th Fleet area of operations.

U.S Navy aircraft routinely fly in the Philippine Sea and have done so for many years. U.S. Navy aircraft and ships will continue to fly, sail and operate anywhere international law allows.

U.S. 7th Fleet is the largest numbered fleet in the world, and with the help of 35 other maritime-nation allies and partners, the U.S. Navy has operated in the Indo-Pacific region for more than a century, providing credible, ready forces to help preserve peace and prevent conflict.

Defense.gov (March, 2020) Department of Defense Statement on People’s Liberation Army Navy Lasing of U.S. Navy P-8A in Unsafe, Unprofessional Manner

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Coronavirus Update: FDA steps to ensure quality of foreign products

We are providing updated and more detailed information about the status of FDA inspections in China and the agency’s oversight of imported products from China, which have been impacted by this outbreak.


Today, we are providing updated and more detailed information about the status of FDA inspections in China and the agency’s oversight of imported products from China, which have been impacted by this outbreak.

While we are not able to conduct inspections in China right now, this is not hindering our efforts to monitor medical products and food safety. We have additional tools we are utilizing to monitor the safety of products from China, and in the meantime, we continue monitoring the global drug supply chain by  prioritizing risk-based inspections in other parts of the world.

The FDA is not currently conducting inspections in China in response to the U.S. Department of State’s Travel Advisory to not travel to China due to the novel coronavirus outbreak. We will continue to closely monitor the situation in China so that, when the travel advisory is changed, we will be prepared to resume routine inspections as soon as feasible.

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We already use other tools to help complement our inspections, including import screening, examinations, sampling, and import alerts, relying on a firm’s previous compliance history, and we use information from foreign governments as part of mutual recognition agreements. Thus, at this time, we can rely on these other tools to give us comprehensive oversight of FDA-regulated products entering this country. This is all part of our agency’s risk-based approach to ensuring quality, as well as compliance with applicable FDA requirements.

It is important to reiterate that inspections are one of many tools that the agency uses to inform our risk strategy for imported FDA-regulated products and to help prevent products that do not meet the FDA’s standards from entering the U.S. market.  A wide variety of FDA-regulated products are imported from China, which makes it important to assure the public of the quality of these products. At this time, over 60% of FDA-regulated products imported from China are medical devices and 20% are housewares (like food packaging).  

In response to the COVID-19 outbreak, the FDA will utilize, where appropriate, our authority to request records from firms “in advance or in lieu of” drug surveillance inspections in China. The Federal Food, Drug, and Cosmetic Act, as amended by the FDA Safety and Innovation Act (FDASIA) of 2012, gives the FDA authority to request records “in advance of or in lieu of” on-site drug inspections.

Congress enacted this provision to improve the effectiveness and efficiency of inspections, given the increasing globalization of drug production.  Along with other FDASIA provisions, this inspection record request authority was viewed as a way to “level the playing field” between foreign and domestic drug inspections by allowing the FDA to review records ahead of time and take a more risk-based approach to conducting both domestic and foreign inspections. These records will help the agency when we resume drug inspections in China.

By applying the use of paper records in our risk-based inspection framework, we can prioritize our early inspections on those deemed most needed, based on the records . By doing so, we hope to rapidly assess what could become a backlog number of on-the-ground surveillance inspections this fiscal year if travel restrictions persist.

In addition to records requests, the FDA will continue working with U.S. Customs and Border Protection to target products intended for importation into the U.S. that violate applicable legal requirements for FDA-regulated products, which may come from a variety of sources, such as first time importers unfamiliar with regulatory requirements or repeat offenders trying to skirt the law. FDA has the ability through our risk-based import screening tool (PREDICT) to focus our examinations and sample collections based on heightened concerns of specific products being entered into U.S. commerce. The PREDICT screening continues to adjust risk scores as necessary throughout the COVID-19 outbreak.  

We are keeping a close eye out for indications of port shopping or cargo diversion and will continue our oversight of shipments through potentially higher-risk venues such as International Mail Facilities. We can refuse admission of products that fail sample testing or may violate other applicable legal requirements.

Fortunately, currently, we are not seeing the impacts of this outbreak resulting in an increased public health risk for American consumers from imported products. There is no evidence to support transmission of COVID-19 associated with imported goods and there have not been any cases of COVID-19 in the United States associated with imported goods. As noted, this remains a dynamic situation and we will continue to assess, and update guidance as needed. 

We also continue to aggressively monitor the market for any firms marketing products with fraudulent COVID-19 prevention and treatment claims. The FDA can and will use every authority at our disposal to protect consumers from bad actors who would take advantage of a crisis to deceive the public, including pursuing warning letters, seizures, or injunctions against products on the market that are not in compliance with the law, or against firms or individuals who violate the law.

We know the public may have questions or concerns for the FDA as a result of this outbreak, including you and your family’s risk of exposure, or whether your critical medical products are safe and will continue to be available in the future.

We assure you that the FDA is working around the clock to monitor and mitigate emerging coronavirus issues through collaborative efforts with U.S. regulators, international partners, and medical product developers and manufacturers to help advance response efforts to combat the COVID-19 outbreak. 

FDA.gov (February, 2020) FDA steps to ensure quality of foreign products

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Confronting the China Threat

China is threatening the U.S. economy—and national security—with its relentless efforts to steal sensitive technology and proprietary information from U.S. companies, academic institutions, and other organizations, FBI Director Christopher Wray said


Director Wray Says Whole-of-Society Response is Needed to Protect U.S. Economic and National Security

China is threatening the U.S. economy—and national security—with its relentless efforts to steal sensitive technology and proprietary information from U.S. companies, academic institutions, and other organizations, FBI Director Christopher Wray said on Thursday.

Wray described the threat from China as “diverse” and “multi-layered.” He noted that the Chinese government exploits the openness of the American economy and society.

“They’ve pioneered an expansive approach to stealing innovation through a wide range of actors,” Wray said during opening remarks at the half-day Department of Justice China Initiative Conference in Washington, D.C.

Wray told the audience that China is targeting everything from agricultural techniques to medical devices in its efforts to get ahead economically. While this is sometimes done legally, such as through company acquisitions, China often takes illegal approaches, including cyber intrusions and corporate espionage.

“They’ve shown that they’re willing to steal their way up the economic ladder at our expense,” he said.

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The FBI is using traditional law enforcement techniques as well as its intelligence capabilities to combat these threats. He said the FBI currently has about 1,000 investigations into Chinese technology theft.

Just last month, a Harvard University professor was charged with lying about his contractual arrangement with China.

Wray also called for a whole-of-society response to these threats. He urged U.S. companies to carefully consider their supply lines and whether and how they do business with Chinese companies. While a partnership with a Chinese company may seem profitable today, a U.S. company may find themselves losing their intellectual property in the long run.

Additionally, U.S. universities should work to protect their foreign students from coercion from foreign governments, Wray said.

Wray noted, however, that these threats do not mean the U.S. shouldn’t welcome Chinese students or visitors.

“What it does mean is that when China violates our criminal laws and well-established international norms, we are not going to tolerate it, much less enable it,” he said. “The Department of Justice and the FBI are going to hold people accountable for that and protect our nation’s innovation and ideas.”

FBI.gov (February, 2020) Confronting the China Threat

Report: Virus-hit Wuhan has two laboratories linked to Chinese bio-warfare program

The Washington Times reported on Friday that the deadly animal virus epidemic spreading globally may have originated in a Wuhan laboratory linked to China’s covert biological weapons program


The Washington Times reported on Friday that the deadly animal virus epidemic spreading globally may have originated in a Wuhan laboratory linked to China’s covert biological weapons program, according to an Israeli biological warfare expert.

Radio Free Asia this week rebroadcast a local Wuhan television report from 2015 showing China’s most advanced virus research laboratory known the Wuhan Institute of Virology, Radio Free Asia reported.

The laboratory is the only declared site in China capable of working with deadly viruses.

The Washington Times reports:

Dany Shoham, a former Israeli military intelligence officer who has studied Chinese bio warfare, said the institute is linked to Beijing’s covert biological weapons program.

“Certain laboratories in the institute have probably been engaged, in terms of research and development, in Chinese [biological weapons], at least collaterally, yet not as a principal facility of the Chinese BW alignment,” Mr. Shoham told The Washington Times.

Work on biological weapons is conducted as part of a dual civilian-military research and is “definitely covert,” he said in an email.

Mr. Shoham holds a doctorate in medical microbiology. From 1970 to 1991 he was a senior analyst with Israeli military intelligence for biological and chemical warfare in the Middle East and worldwide, holding the rank of Lieutenant Colonel.

China in the past has denied having any offensive biological weapons. The State Department, in a report last year, said it suspects China has engaged in covert biological warfare work.

A Chinese Embassy spokesman did not return an email seeking comment.

Chinese authorities so far have said the origin of the coronavirus that has killed scores and infected hundreds in in central Hubei Province is not known.

Meanwhile, the Centers for Disease Control and Prevention (CDC) is closely monitoring the outbreak of respiratory illness caused by a novel (new) coronavirus (termed “2019-nCoV”) that was first detected in Wuhan City, Hubei Province, China and which continues to expand. Chinese health officials have reported hundreds of infections with 2019-nCoV in China, including outside of Hubei Province.

Infections with 2019-nCoV also are being reported in a growing number of countries internationally, including the United States, where the first and second 2019-nCoV infections were reported on January 21 and January 24, 2020, respectively, both in travelers returning from Wuhan.

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