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B-421748 Jul 28, 2023 1 (2023-07-28)

handle is hein.gao/gaoozs0001 and id is 1 raw text is: 



                   U.S. GOVERNMENT   ACCOUNTABILITY OFFICE
441 G St. N.W.                                                 Comptroller General
Washington, DC 20548                                            of the United States




Decision


Matter of:  Beckman  Coulter, Inc.

File:       B-421748

Date:       July 28, 2023

Thomas  M. Holl, Beckman Coulter, Inc., for the protester.
Andrew  J. Smith, Esq., Natalie W. McKiernan, Esq., Blaine L. Hutchison, Esq., Seth
Ritzman, Esq., and Nhu T. Tran, Esq., Department of the Army, for the agency.
Cree W. Townsend,  Emily R. O'Hara, Esq., and Peter H. Tran, Esq., Office of the
General Counsel, GAO, participated in the preparation of the decision.
DIGEST

Protest challenging the awardee's technical acceptability is dismissed as untimely
where the protest was filed more than 10 days after the protester received the
information that formed the basis of protest.
DECISION

Beckman  Coulter, Inc., of Indianapolis, Indiana, protests the award of a contract to
Sysmex  America, Inc., of Lincolnshire, Illinois, under request for quotations (RFQ)
No. W81 K00-22-Q-0109, issued by the Department of the Army, Army Medical
Command,   for laboratory equipment and maintenance services for flow cytometry
testing. The protester alleges the award was improper because the awardee should
have been found to be technically unacceptable.

We  dismiss the protest as untimely.

BACKGROUND

The Army  issued the RFQ on July, 14, 2022, using the simplified acquisition procedures
for the purchase of commercial items prescribed in subpart 13.5 of the Federal
Acquisition Regulation (FAR), for laboratory equipment and flow cytometry testing at the
San Antonio Military Medical Center, Fort Sam Houston, Texas. Req. for Dismissal
(RFD) at 1; RFD, exh. 1, RFQ at 60. The RFQ anticipated that award would be made
on a lowest-priced, technically acceptable (LPTA) basis. RFQ at 95. As relevant here,
the solicitation required all testing materials to be Food and Drug Administration (FDA)
approved platforms. RFQ at 52.

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