WAC 16-256-040
Testing requirements for processed animal
waste products. (1) The purpose of the sampling and testing
requirements in this section is to determine the presence of
harmful materials or biological contaminants specified in WAC 16-256-070 and to assure compliance with the quality standards
in that section.
(2) Any person seeking or maintaining a commercial feed
license for any processed animal waste product facility must:
(a) Test those products, by representative sampling;
(b) Analyze those samples; and
(c) Keep accurate records of the test results for two
years.
(3) The sample used must be of sufficient size to provide
meaningful data that is statistically reliable.
(4) Before a processed animal waste product is
distributed, the licensee must comply with the following
sample and analyses requirements:
(a) Sufficient testing and analyses must be conducted to
ensure that the last three consecutive production runs are
consistent with the required quality standards in WAC 16-256-070.
(b) After the initial testing is completed, periodic
analyses (at least one analysis each calendar quarter) must be
conducted on subsequent production runs. Less frequent
testing may be allowed when the analytical results show
continued uniformity and a consistent margin of compliance.
More frequent tests must be conducted when the analytical
results show either a wide range of levels or levels close to
established quality standard limits.
(5) Analysis of the samples used to determine if the
processed animal waste meets the quality standards in WAC 16-256-070 must also include the following:
(a) Drugs used (or suspected of use) in feed or as a
therapeutic treatment of the animals;
(b) Pesticides used on the animal, facilities, and wastes
for pest control;
(c) Pathogenic organisms, at least to include Salmonella
and E. coli;
(d) Heavy metals, including, but not limited to, arsenic,
cadmium, copper, lead, mercury and selenium;
(e) Parasitic larva or ova; and
(f) Mycotoxins, such as aflatoxins.
(6) Sequential testing is required when the periodic
analyses required by WAC 16-256-040(4) or other information
available to the manufacturer of the ingredient indicates
that:
(a) The ingredients are not within the limitations
established in these regulations;
(b) Changes are made in the manufacturing process;
(c) New or expanded sources of the raw ingredients are
used; or
(d) Changes occur in the drugs or pesticides used by the
supplier(s) of the raw ingredient(s).
[Statutory Authority: Chapters 15.53 and 34.05 RCW. 03-23-131, § 16-256-040, filed 11/19/03, effective 7/1/04.]