[Code of Federal Regulations]
[Title 9, Volume 1]
[Revised as of January 1, 2007]
From the U.S. Government Printing Office via GPO Access
[CITE: 9CFR71.21]

[Page 226-228]
 
                  TITLE 9--ANIMALS AND ANIMAL PRODUCTS
 
  CHAPTER I--ANIMAL AND PLANT HEALTH INSPECTION SERVICE, DEPARTMENT OF 
                               AGRICULTURE
 
PART 71_GENERAL PROVISIONS--Table of Contents
 
Sec. 71.21  Tissue and blood testing at slaughter.

    (a) Any person moving livestock or poultry interstate for slaughter 
or rendering may only move the animals to a slaughtering establishment 
or a rendering establishment that has been

[[Page 227]]

listed by the Administrator \8\ for the purposes of this part. Livestock 
or poultry may not be removed from the premises of a slaughtering 
establishment or a rendering establishment listed by the Administrator 
except under a permit issued by APHIS, and in accordance with applicable 
FSIS regulations in this title. A slaughtering establishment or 
rendering establishment may receive livestock or poultry in interstate 
commerce only if the establishment has been listed by the Administrator. 
The Administrator may list a slaughtering establishment or a rendering 
establishment after determining that collecting samples for testing from 
the establishment is not currently necessary for the purposes of APHIS 
disease surveillance programs and the establishment has agreed to allow 
testing and to provide the access and facilities required by this 
section upon future APHIS notification that testing is required at the 
establishment. The Administrator will list a slaughtering or rendering 
establishment after determining that it meets the following facility and 
access requirements:
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    \8\ A list of these slaughtering or rendering establishments may be 
obtained by writing to National Center for Animal Health Programs, VS, 
APHIS, 4700 River Road Unit 43, Riverdale, MD 20737-1231.
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    (1) The establishment provides space and equipment in accordance 
with paragraph (b) of this section \9\ within their facility for blood 
and tissue sample collection;
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    \9\ FSIS also has equipment and space requirements for official 
establishments at Sec. 307.2(c) of this title.
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    (2) The establishment allows APHIS, FSIS, or APHIS contractors to 
take blood and tissue samples from all livestock or poultry at the 
facility without cost to the United States, and specifically allows 
these personnel access to the processing line to collect samples; and
    (3) The establishment allows APHIS, FSIS, or APHIS contractors to 
record the identification of individual animals and retain any external 
or internal identification devices.
    (b) The establishment must provide office and sample collection 
space, including necessary furnishings, light, heat, and janitor 
service, rent free, for the use by APHIS, FSIS, or APHIS contractors 
collecting samples for blood and tissue testing under this section. The 
Administrator will inform each establishment of the exact amount and 
type of space required, taking into account whether APHIS will be 
conducting complete tests at the facility, or only collecting samples 
and sending them elsewhere for testing. At the discretion of the 
Administrator, small plants need not furnish facilities as prescribed in 
this section if adequate facilities exist in a nearby convenient 
location. In granting or denying listing of an establishment, the 
Administrator will consider whether the space at the facility:
    (1) Is conveniently located, properly ventilated, and provided with 
lockers suitable for the protection and storage of supplies;
    (2) Has sufficient light to be adequate for proper conduct of sample 
collection and processing;
    (3) Includes racks, receptacles, or other suitable devices for 
retaining such parts as the head, glands, and viscera, and all parts and 
blood to be collected, until after the post-mortem examination is 
completed;
    (4) Includes tables, benches, and other equipment on which sample 
collection and processing are to be performed, of such design, material, 
and construction as to enable sample collection and processing in a 
safe, ready, efficient, and clean manner;
    (5) Has adequate arrangements, including liquid soap and cleansers, 
for cleansing and disinfecting hands, dissection tools, floors, and 
other articles and places that may be contaminated by diseased carcasses 
or otherwise; and
    (6) Has adequate facilities, including denaturing materials, for the 
proper disposal in accordance with this chapter of tissue, blood, and 
other waste generated during test sample collection.
    (c) The Administrator will give the operator of the establishment 
actual notice that APHIS, FSIS, or an APHIS contractor will be taking 
blood and/or tissue samples at the establishment. The Administrator may 
give the operator of the establishment notice in any

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form or by any means that the Administrator reasonably believes will 
reach the operator of the establishment prior to the start of sample 
collection.
    (1) The notice will include the anticipated date and time sample 
collection will begin. The notice will also include the anticipated 
ending date and time.
    (2) The Administrator will give the operator of the establishment as 
much advance notice as possible. However, the actual amount of notice 
will depend on the specific situation.
    (d) Denial and withdrawal of listing. The Administrator may deny or 
withdraw the listing of an establishment upon a determination that the 
establishment is not in compliance with the requirements of this 
section.
    (1) In the case of a denial, the operator of the establishment will 
be informed of the reasons for the denial and may appeal the decision in 
writing to the Administrator within 10 days after receiving notification 
of the denial. The appeal must include all of the facts and reasons upon 
which the person relies to show that the establishment was wrongfully 
denied listing. The Administrator will grant or deny the appeal in 
writing as promptly as circumstances permit, stating the reason for his 
or her decision. If there is a conflict as to any material fact, a 
hearing will be held to resolve the conflict. Rules of practice 
concerning the hearing will be adopted by the Administrator.
    (2) In the case of withdrawal, before such action is taken, the 
operator of the establishment will be informed of the reasons for the 
proposed withdrawal. The operator of the establishment may appeal the 
proposed withdrawal in writing to the Administrator within 10 days after 
being informed of the reasons for the proposed withdrawal. The appeal 
must include all of the facts and reasons upon which the person relies 
to show that the reasons for the proposed withdrawal are incorrect or do 
not support the withdrawal of the listing. The Administrator will grant 
or deny the appeal in writing as promptly as circumstances permit, 
stating the reason for his or her decision. If there is a conflict as to 
any material fact, a hearing will be held to resolve the conflict. Rules 
of practice concerning the hearing will be adopted by the Administrator. 
However, withdrawal shall become effective pending final determination 
in the proceeding when the Administrator determines that such action is 
necessary to protect the public health, interest, or safety. Such 
withdrawal shall be effective upon oral or written notification, 
whichever is earlier, to the operator of the establishment. In the event 
of oral notification, written confirmation shall be given as promptly as 
circumstances allow. This withdrawal shall continue in effect pending 
the completion of the proceeding, and any judicial review thereof, 
unless otherwise ordered by the Administrator.

(Approved by the Office of Management and Budget under control number 
0579-0212.)

[69 FR 10150, Mar. 4, 2004]