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Oct

15

Agreement Guidelines Update Updated


Posted by at 7:37 pm on October 15, 2009
Category: DDTC

State DepartmentEarlier this week, we reported on the new Agreement Guidelines posted last Friday by the Directorate of Defense Trade Controls (“DDTC”). The new Guidelines provided instructions for electronic filing of requests for approval of agreements to exchange technical data on military items with foreigners (“TAAs”) and agreements for the manufacture of military items overseas (“MLAs”).

One source of concern was the new format announced for filing amendments to these agreements. Although not stated clearly in the new guidelines, DDTC has advised us that the new format, although permissible now, will only become mandatory when electronic filing becomes mandatory in 2010. In the meantime, exporters can still file amendments in the old format — at least if they still have a hard copy of the earlier guidelines which described the old format since those guidelines have disappeared from DDTC’s website.

Another clarification was provided with respect to the requirement that conformed copies of the agreement be submitted with the amendment. DDTC, in describing those conformed copies, stated:

DDTC will only accept amendments that have been “conformed” or consolidated. In other words, all major amendments MUST be submitted as entire agreements with proposed changes identified by bolded text (not “track changes”). Applications that simply describe which sections or articles to the agreement are being modified shall be Returned Without Action

We wondered how all changes, both insertions and deletions, could be bolded without unnecessary confusion. DDTC told us today that additions should be bolded in the conformed copy of the agreement and that deleted sections should simply be deleted, with each deletion being described in the part of the amendment that summarizes the changes accomplished by the amendment. That’s not what the new guidelines say, but it is certainly easier and clearer than bolding all changes in the conformed copy.

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Copyright © 2009 Clif Burns. All Rights Reserved.
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Oct

14

Think Positive


Posted by at 7:31 pm on October 14, 2009
Category: Anti-Boycott

Boycotting the BoycottPerhaps in order to remind everyone that it still exists, the the Bureau of Industry and Security’s Office of Anti-Boycott Compliance (“OAC”) issued a warning letter to CENTRIA, a manufacturer of building enclosure systems based in Moon Township, Pennsylvania. According to the letter, CENTRIA supplied to its freight forwarder a commercial invoice with the following language:

THE GOODS SHIPPED ARE NOT OF ISRAELI ORIGIN NOR DO THEY CONTAIN ANY ISRAELI MATERIALS. THEY ARE NOT DESIGNATED TO VISIT ANY ISRAELI PORTS NOR ARE THEY EXPORTED FROM ISRAEL. THEY ARE OF USA ORIGIN.

The OAC said it was closing the matter with just a warning letter because CENTRIA had voluntarily disclosed the violation.

As usual, the OAC provided little commentary as to why this language was problematic and merely asserted simply that “Section 760.2(d) of the Regulations prohibits providing such information.” OAC’s bare bones explanation is certainly not the result of OAC being too busy to spend the time explaining its reasoning. Perhaps it’s an admission that the Anti-Boycott regulations, with their 101 pages of densely packed legalese and eleventy trillion or so hypothetical examples of what’s naughty and what’s nice, are simply too complex to explain and summarize in any meaningful sense in less than, well, a hundred or so pages.

The problem here is that the absence of such an explanation, even a brief one, might give the wrong impression to exporters. The letter could be read as saying that the regulations prohibit supplying the information that the goods are made in the U.S.A. The warning letter might have at least provided an explanation of the difference between a negative certificate of origin (mostly naughty) and a positive certificate of origin (mostly nice). A positive certificate of origin is generally acceptable unless the person supplying that certificate knows that it is being used to enforce a boycott as, for example, when the request for the positive certificate comes from an anti-boycott compliance office of an Arab League country.

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Copyright © 2009 Clif Burns. All Rights Reserved.
(No republication, syndication or use permitted without my consent.)

Oct

13

New Agreement Guidelines Posted by DDTC


Posted by at 7:42 pm on October 13, 2009
Category: DDTC

State DepartmentOn Friday the Directorate of Defense Trade Controls (“DDTC”) issued revised guidelines for submitting agreements such as Technical Assistance Agreements (“TAA”) and Manufacturing License Agreements (“MLA”). As most export geeks know, TAAs and MLAs, once submitted to and approved by DDTC, permit, respectively, the exchange of technical data on defense articles with foreigners and the manufacture of defense articles overseas.

Most of the changes in the revised guidelines relate to matters relating to the long-awaited electronic submission of TAAs and MLAs though DDTC’s electronic filing system. Electronic filing of agreements will become mandatory in 2010. After reviewing these new guidelines for electronic submission, my guess is that most exporters would be happy to wait more, a long time more, maybe a decade or so, in fact, for electronic filing of agreements.

What DDTC has managed to do is to make electronic filing even more complicated and difficult than paper filing. Not only must the exporter file everything that it had previously been submitting, including the tediously ornate transmittal letter, but also the exporter must now complete and file with all that a DSP-5 which, in this case, DDTC quaintly calls a “vehicle DSP-5.” Why on earth DDTC can’t simply let exporters upload pdf versions of the agreement documents (a filing procedure used successfully by, for example, almost every court in the country) is unclear. Instead, by adding an additional layer of paperwork, DDTC has just made the procedure more expensive and time-consuming as well as creating the opportunity for mistakes and returned agreements.

Not everything in the new guidelines relates to electronic filing. Some of the changes relate to paper filings before electronic filing becomes mandatory. For example, amendments must now contain a “conformed” copy of the agreement with the changes in bold typeface. The guidelines make clear that “tracked” changes (i.e. additions underlined and deletions stricken out) aren’t acceptable, so it is not entirely clear how DDTC wants agreement filers to indicate the difference between additions and deletions, nor why it is so adamant about not wanting “tracked” changes. Perhaps the computers at DDTC can’t render strikeout text.

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Copyright © 2009 Clif Burns. All Rights Reserved.
(No republication, syndication or use permitted without my consent.)

Oct

8

Spy Games


Posted by at 8:04 pm on October 8, 2009
Category: Criminal PenaltiesEconomic Sanctions

Dawn HannaIn March, Dawn Hanna was convicted by a jury in Detroit for exporting mobile telecom equipment to Saddam Hussein in violation of the U.S. embargo against Iraq in place at the time of the export. Hanna claimed throughout her trial that the purchaser of the equipment told her that the end user was in Turkey. The government’s sentencing memo, however, cited a number of communications and emails from Hanna where she seemed quite aware that the items were destined for Iraq and not Turkey.

The case, however, recently took an interesting turn of sorts. Apparently the person who approached Hanna to purchase the equipment, a Jordanian named Emad al-Yawer, has come forward and claimed that he was working for the CIA when he approached Hanna. According to al-Yawer, in an affidavit filed in April, the CIA wanted to alter the equipment to track Saddam and listen to his conversations. As al-Yawer said somewhat more colorfully in a recent interview with a Detroit television station:

The whole idea was, once they get to Saddam, send a smart bomb and blow him into smithereens

The judge apparently did not find the new evidence sufficient to grant Hanna a new trial. Prosecutors in the case have said that the new evidence remains under seal, although apparently a redacted version of the al-Yawer affidavit is available on a website set up by Dawn Hanna’s parents.

Of course, the interesting question here is whether it matters at all that al-Yawer was working for (or with) the CIA. Even if he was cooperating with the CIA, the efforts by Hanna’s defenders to say that the sale of the equipment to Hussein was the government’s fault doesn’t seem that convincing. Certainly this argument wouldn’t have been convincing if the purchaser was an undercover U.S. government agent. I suppose that if the alleged CIA agents had directed al-Yawer to buy the equipment from Hanna, this argument might have some legs. Similarly, if the CIA had contacted Hanna directly, identified themselves as CIA agents, enlisted her help in exporting the equipment, and then had her prosecuted, Hanna might have an argument. But there is no evidence that any of this happened.

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Copyright © 2009 Clif Burns. All Rights Reserved.
(No republication, syndication or use permitted without my consent.)

Oct

7

OFAC Guidance Imposes New Burdens on Exports of Medical Devices


Posted by at 11:47 pm on October 7, 2009
Category: OFAC

Star Trek Dermal RegeneratorThe Treasury Department’s Office of Foreign Assets Control (“OFAC”) issued a guidance today on exports of medical parts to support medical devices legally exported under OFAC licenses to Iran or Sudan, the two countries for which OFAC exercises licensing authority over medical devices. And, not surprisingly, OFAC continues its efforts to resist the mandate of the Trade Sanctions Reform and Export Enhancement Act of 2000, which sought, on obvious humanitarian grounds, to prevent OFAC and other export agencies, from restricting exports of food, medicine and medical devices to sanctioned countries.

Under the new guidance, rather than saying simply that exports of replacement parts are ordinarily incident to the export of medical device itself, and therefore allowed, OFAC imposes burdensome conditions on those exports. The potential impact of this red tape on ordinary citizens in Iran and Sudan who are sick or dying just doesn’t matter. Worse, such punitive measures directed at the sick and dying are not going to cause Iran to give up its nuclear aspirations or cause the regime in Sudan to rethink its genocidal policies.

First, if the part that needs to be replaced fails during the one-year period of validity of the export license for the medical device itself, the part can be exported, but only as a one-for-one replacement. But there is another, and more significant, catch. The replacement part must have obtained a specific classification as EAR99 from the Bureau of Industry and Security (“BIS”). And even if the exporter has a classification for the medical device as EAR99, it doesn’t count unless that classification specifically mentions the replacement part in question.

Medical devices on this list don’t require a specific BIS classification, but the list doesn’t include parts. So even though an OFAC license for a digital blood pressure monitor doesn’t require a specific classification from BIS, exporting a replacement display screen for that device does!

Second, if the underlying license has expired, a new OFAC license is required to export the replacement parts. And, again, a specific BIS classification is required for each of the replacement parts exported, even if the device itself was classified as EAR99 or was on the exempted list and did not require a BIS classification. OFAC license approvals can take from 40 days to six months or more, which means that patients may go without care while the exporter waits for a BIS classification and an OFAC license.

Third, even an import of the device back to the United States for repair will require a license — as will the re-export after the device is repaired. The application will require, among other things, a “statement regarding the circumstances under which the medical device broke.” It’s not clear that simply saying that the device was being used and it just failed will suffice as a justification for a license.

If you are an exporter of medical devices under TSRA licenses to either Iran or Sudan, you should make sure that any request for a required BIS classification of the device also includes a request for classification of the important parts of that device. You also should be aware that you can’t solve this problem by continually renewing the license. Parts can only be shipped without a license under this guidance if they are shipped during the original period of validity of the license under which the medical device for which the parts are destined was exported.

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Copyright © 2009 Clif Burns. All Rights Reserved.
(No republication, syndication or use permitted without my consent.)