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1)
Producer maintains a record of any pesticide or herbicide
use that could cause a violative residue in grazing cattle
or feedlot cattle. A record of storage should be maintained
for reference.
2) Only
FDA approved medicated feed additives will be used in
rations.
3) All
medicated feed additives will be used in accordance with the
FDA approved label. Extra-label use of feed additives is
strictly prohibited.
4)
Operator will document that all additives are withdrawn at
the proper time to avoid violative residues.
5) If
the beef operation formulates medicated rations, a formula
record of all medicated feed rations produced will be kept.
Production records of all batches of feed produced which
contain medicated feed additives, including date run, ration
name or number, amount produced, and lots receiving the feed
will be recorded.
6)
Keep all records for not less than two years from the date
of transfer or sale of the cattle.
7) No
ruminant-derived protein sources can be fed. This includes
meat and bone meal. Other ruminant-derived products such as
blood by-products and tallow can be used consistent with FDA
regulations.
8) The
same facility and equipment will not be used to manufacture,
store or transport both non-packaged ruminant livestock feed
and feeds containing prohibited animal proteins. Storage may
occur in the same facility if a wall separates prohibited
and non-prohibited products.
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