Two
days later in a press briefing, President Trump formally
announced that the federal government had begun to use the DPA, as
previously stated in the EO to direct US companies to shift their focus on
producing emergency supplies of protective masks and other necessary medical
devices.
What
is the Defense Production Act?
The
Defense Production Act (DPA) was initially enacted in 1950 during the Korean
war to grant the president the authority to direct what the private sector can
produce in the interest of national defense. If the DPA is invoked by the
president, federal agencies have the authority to direct domestic industrial
entities to produce essential goods and materials necessary for national
defense.
Through
this Act, the US Department of Defense has historically requested private
companies to assist in military readiness, but the Act has been amended over
time to broaden the scope beyond that to include essential goods and materials
needed for recovery and response to natural hazards and other national
emergencies. President Trump EO from March 18, 2020 invoked
this Act which had three sections detailing how it would come into effect.
FEMA’s
Temporary Halt
The Federal Emergency Management Agency (FEMA) is issued a temporary rule to allocate certain scarce or
threatened materials for domestic use, so that these materials may not be
exported from the United States without explicit approval by FEMA. The rule
covers five types of personal protective equipment (PPE):
- N95 Filtering Facepiece
Respirators, including devices that are disposable half-face-piece
non-powered air-purifying particulate respirators intended for use to
cover the nose and mouth of the wearer to help reduce wearer exposure to
pathogenic biological airborne particulates;
2.
Other Filtering Facepiece Respirators
(e.g., those designated as N99, N100, R95, R99, R100, or P95, P99, P100),
including single-use, disposable half-mask respiratory protective devices that
cover the user’s airway (nose and mouth) and offer protection from particulate
materials at an N95 filtration efficiency level per 42 CFR 84.181;
3.
Elastomeric, air-purifying respirators
and appropriate particulate filters/cartridges;
4.
PPE surgical masks, including masks
that cover the user’s nose and mouth and provide a physical barrier to fluids
and particulate materials; and
5.
PPE gloves or surgical gloves,
including those defined at 21 CFR 880.6250 (exam gloves) and 878.4460 (surgical
gloves) and such gloves intended for the same purposes.
While this rule remains in effect no shipments of the five types
of PPE may be exported from the United States without explicit approval by
FEMA.
This temporary rule is scheduled to be published in the Federal
Register on April 10, 2020, at which point it would become effective until 120
days after date of publication in the Federal Register. Once in effect, it will
amend FEMA’s preparedness regulations and that includes the types of PPE the
temporary rule aims to restrict exports for, which had already been laid out in
a previous presidential memoranda from April 3, 2020. FEMA issued their
temporary rule drawing authority from the DPA, multiple EOs, and the memoranda.
What is the Process to Export these Products?
From all the information provided so far, no federal export
control agencies are involved in this process, meaning FEMA has developed their
own process for authorization of the exports.
According to the temporary rule, the process is as follows:
·
Customs and Border Protection (CBP) will notify
FEMA of any intended exports of the restricted PPE.
·
CBP would then temporarily detain the export
while the FEMA administrator decides whether to return the shipment for
domestic use or issue a rated order for part or all of the shipment.
·
The FEMA administrator makes a decision within a
reasonable time frame after CBP notifies of the intended export.
·
If it is decided the shipment is needed for
domestic use, FEMA will purchase the shipment.
Potential
Penalties
The FEMA
administrator may apply for a preliminary, permanent, or temporary injunction,
restraining order, or other order to enforce compliance. Any violations are
subject to penalties available under section 103 of the DPA. The criminal and
civil penalties are a potential $10,000 fine and/or one year of imprisonment.
Penalties under 18
U.S.C. 554 are also applicable and criminal with a potential 10 years’
imprisonment and/or a fine.
The
FEMA administrator has authority under section 705 of the DPA, with adequate
scope and purpose, to:
·
Conduct investigations;
·
Request information or testimony; and
·
Inspect records or premises;
The
administrator, with their judgment, would determine if any person has engaged
or is about to engage in acts or practices to violate any provisions of the
temporary rule to proceed accordingly with penalties.
Allocation of Intended PPE Exports
FEMA has established criteria to determine whether or not to
allocate PPE for domestic use and will consider the following factors:
·
The need to ensure that scare or threatened
items are appropriately allocated for domestic use;
·
Minimization of disruption to the supply chain,
both domestically and abroad;
·
The circumstances surrounding the distribution
of the materials and potential hoarding or price-gouging concerns;
·
The quantity and quality of the materials;
·
Humanitarian considerations; and
·
International relations and diplomatic
considerations.
What Exemptions Exist?
An important
exemption to note is that U.S. manufacturers can apply to FEMA for an exemption
if they meet the following criteria:
1.
The U.S. manufacturer has a continuous export agreement in place since
at least January 1, 2020.
2.
At least 80 percent of the manufacturer’s
domestic production was distributed in the US in the preceding 12 months.
It
is important to note that even if you qualify for the exemption, FEMA can waive
this exemption if the FEMA administrator deems it necessary or appropriate for
the promotion of national defense.
FEMA will have authority to decide whether an export
qualifies for the exemption and exporters cannot make this determination on
their own. FEMA will continue to work with CBP through this exemption process.
On
April 9, 2020, CBP published a memorandum superseding the one published on
April 4th. This memorandum serves as an updated guidance for the
allocation of certain scarce or threatened health and medical resources for
domestic use. The focus of the allocation is on commercial quantities defined
as shipments valued at $2,500 and containing more than 10,000 units of gloves,
masks, or other commodities referenced above. In the Memo, CBP noted that the
following circumstances also qualify for an exclusion to the export ban:
·
Exports to Canada or Mexico;
·
Exports to U.S. Government entities such as U.S.
military bases overseas;
·
Exports by U.S. Government agencies;
·
Exports by U.S. charities;
·
Exports by critical infrastructure industries
for the protection of their workers;
·
Exports by the 3M Company;
·
Express or Mail Parcels that do not meet the
commercial quantity definition above;
·
In-transit shipments.
Export
shipments that do not meet the exclusions would receive document reviews and
physical examinations conducted at the port to determine if the commodity fits
the definition of scarce or threatened. Only when commodity expertise is
required should there be consultation with the COVID-19 Cargo Resolution Team.
Diaz
Trade Law specializes in customs and international trade matters. Our Customs
and International Trade Law attorneys are available at info@diaztradelaw.com or 305-456-3830.
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