Diagnostic Products Corporation Announces Annual Meeting Date
17 Juin 2005 - 2:00PM
Business Wire
Diagnostic Products Corporation (NYSE:DP) today announced that it
will hold its annual meeting of shareholders on September 8, 2005.
The record date to determine the shareholders entitled to receive
notice of the meeting and to vote at the meeting will be July 15,
2005. Shareholders interested in submitting a proposal for
inclusion in the Company's proxy statement for the annual meeting
must submit such proposal to the Company no later than July 8,
2005, and must otherwise comply with the requirements of SEC Rule
14a-8. In addition, the proxy solicited by the Board of Directors
for the annual meeting will confer discretionary authority to vote
on any shareholder proposal presented at the meeting other than
pursuant to Rule 14a-8, unless the Company receives notice of such
proposal on or before July 8, 2005. Shareholder proposals should be
addressed to the Secretary of the Company at its executive offices
located at 5210 Pacific Concourse Drive, Los Angeles, California
90045. Diagnostic Products Corporation, founded in 1971, is the
global leader dedicated exclusively to immunodiagnostics. DPC's
product menu includes over 75 immunoassays and more than 360
specific allergens and allergy panels. In addition, DPC addresses
the chemistry and laboratory automation testing needs of its
customers through partnerships with manufacturers of chemistry
systems and reagents. The combined chemistry and immunoassay menu
is one of the largest and most diversified available, covering most
laboratory tests requested. DPC also designs and manufactures
automated laboratory instrumentation, which provides fast, accurate
results while reducing labor and reagent costs. DPC sells its
products to hospitals, clinics and laboratories in more than 100
countries. Additional Company information can be found on DPC's
website at www.dpcweb.com. Except for the historical information
contained herein, this press release contains forward-looking
statements that involve risks and uncertainties that could cause
actual results to differ materially. These factors include the
effects of governmental or other actions relating to the FDA's
decision that its Application Integrity Policy should be applied to
the Company or relating to the Company's Chinese affiliate; the
rate of customer demand for the Company's products; the Company's
ability to successfully market new and existing products; its
dependence on certain suppliers; domestic and foreign government
regulation; its ability to keep abreast of technological
innovations and to translate them into new products; competition;
political and economic instability in certain markets including the
movements of foreign currencies relative to the dollar; and other
risks and uncertainties disclosed from time to time in the
Company's SEC reports and filings.
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