St. Jude Medical v. Comm'r

97 T.C. No. 33, 97 T.C. 457, 1991 U.S. Tax Ct. LEXIS 93
CourtUnited States Tax Court
DecidedOctober 31, 1991
DocketDocket No. 5274-89
StatusPublished
Cited by17 cases

This text of 97 T.C. No. 33 (St. Jude Medical v. Comm'r) is published on Counsel Stack Legal Research, covering United States Tax Court primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
St. Jude Medical v. Comm'r, 97 T.C. No. 33, 97 T.C. 457, 1991 U.S. Tax Ct. LEXIS 93 (tax 1991).

Opinion

OPINION

WRIGHT, Judge:

Respondent determined the following deficiencies in petitioner’s Federal income taxes:

Year Deficiency
1979. $194,794
1981. 233,956
1982. 812,906
1983. 832,559

After concessions, the deficiency determined for taxable year 1979 is no longer in issue. The issues remaining for decision with respect to taxable years 1981, 1982, and 1983 are:

(1) Whether the research and development expense allocation moratorium under section 223 of the Economic Recovery Tax Act of 1981 (sec. 223 of ERTA), Pub. L. 97-34, 95 Stat. 172, 249, is applicable to the computation of combined taxable income;

(2) whether research and development expenses attributable to medical devices which were never placed into production or offered for sale are allocable and apportion-able as provided by section 1.861-8(e)(3), Income Tax Regs., in computing combined taxable income for purposes of the domestic international sales corporation (DISC) intercompany pricing rules and, if so;

(3) whether section 1.861-8(e)(3), Income Tax Regs., as incorporated by section 1.994-l(c)(6)(iii), Income Tax Regs., for purposes of the DISC intercompany pricing rules, is an invalid regulation:

(a) to the extent it requires allocation of research and development expenses using Standard Industrial Classification (SIC) product categories for the computation of combined taxable income;

(b) to the extent it prohibits an allocation of research and development expenses using industry and trade usage product categories;

(c) to the extent it precludes the use of the “wholesale trade category” in allocating research and development expenses; and

(d) to the extent it precludes the use of the “exclusive geographic apportionment method” in apportioning research and development expenses.

The parties submitted this case fully stipulated pursuant to Rule 122.1 The stipulation of facts, supplemental stipulation of facts, and attached exhibits are incorporated herein.

Petitioner, a Minnesota corporation, had its principal place of business in St. Paul, Minnesota, when its petition was filed. Petitioner is an accrual basis, calendar year taxpayer which develops, manufactures, and sells medical products. Petitioner’s only product during the years at issue was an artificial heart valve. Generally, in the medical products business foreign sales precede domestic sales because of the time required to obtain Food and Drug Administration clearance to market medical products in the United States. Petitioner obtained clearance to market its heart valves in the United States on December 17, 1982.

On December 20, 1979, petitioner initiated a research and development project in order to produce a cardiac pacemaker. Due to escalating costs and startup problems, petitioner terminated its effort to develop the cardiac pacemaker in March of 1981. In April of 1980, petitioner entered into a joint research and development project in order to produce an implantable insulin pump. Petitioner abandoned its effort to develop implantable insulin pumps in 1983. No sales of a cardiac pacemaker or insulin pump were ever attempted by petitioner or its subsidiaries. Cardiac pacemakers, insulin pumps, and heart valves constitute separate products or product lines under recognized industry or trade usage in the medical goods manufacturing industry.

On April 20, 1980, petitioner incorporated St. Jude International Sales Corp. (International), a wholly owned subsidiary, for the purpose of qualifying it as a DISC and obtaining the tax deferral advantages available pursuant to the DISC provisions. International, an accrual basis taxpayer, operated on a January 31 fiscal year. Pursuant to a DISC commission agreement, petitioner was to pay International the maximum commission allowable under section 994 and the applicable regulations for all export sales of petitioner’s product. International qualified as a DISC under section 992 during its fiscal years 1981 through 1984. International incurred no research and development expenses during the years in issue.

Petitioner’s total sales, domestic sales, export commission sales, and the percentage of export commission sales to total sales during calendar year 1981, 1982, and 1983 were:

Total Domestic
Year sales sales
1981 $13,206,395 $4,953,507
1982 17,528,098 6,285,996
1983 25,624,428 11,847,468
Export commission sales involving International $8,252,888 11,242,102 13,776,960
% of export sales to total sales 62.48% 64.14 53.76

During each year at issue, 100 percent of petitioner’s research and development activity was performed in the United States. Because the terms of sale for International were f.o.b., St. Paul, Minnesota, International bore the expense and risk of loss of putting a shipment into possession of the carrier.

A preliminary requirement in determining the tax deferral benefits available to petitioner through section 944(a)(2) of the DISC intercompany pricing rules is the computation of the “combined taxable income” of petitioner and International. Combined taxable income equals the excess of the gross receipts of the DISC from export commission sales over the total costs of the DISC and its related supplier (petitioner) which relate to the gross receipts. In computing combined taxable income, petitioner failed to allocate any of the research and development expenses attributable to the cardiac pacemaker and the insulin pump to gross receipts from export sales. In addition, petitioner failed to allocate 30 percent of the research and development expenses attributable to the heart valve between gross receipts from export sales and all other gross receipts:

R&D Allocated Exclusively to All Other Gross Receipts
Description
Implantable insulin pump Implantable cardiac pacemaker 30% exclusive apportionment Cost of terminating implantable insulin pump development Total
International fiscal year ending
1/31/82 1/31/83 1/31/84
$390,217 390,121
87,719 $451,123 $552,200
655,806
1,523,863 451,123 552,200

Respondent recomputed combined taxable income by allocating additional research and development expenses between gross receipts from export sales and all other gross receipts:

Free access — add to your briefcase to read the full text and ask questions with AI

Related

Boeing Co. v. United States
258 F.3d 958 (Ninth Circuit, 2001)
General Dynamics Corp. v. Commissioner
108 T.C. No. 9 (U.S. Tax Court, 1997)
General Elec. Co. v. Commissioner
1995 T.C. Memo. 306 (U.S. Tax Court, 1995)
International Paper Co. v. United States
33 Fed. Cl. 384 (Federal Claims, 1995)
Apollo Computer, Inc. v. United States
32 Fed. Cl. 334 (Federal Claims, 1994)
Perkin-Elmer Corp. v. Commissioner
103 T.C. No. 26 (U.S. Tax Court, 1994)
Bowater, Inc. v. Commissioner
101 T.C. No. 14 (U.S. Tax Court, 1993)
Intel Corp. v. Commissioner
100 T.C. No. 39 (U.S. Tax Court, 1993)
Napp Sys., Inc. v. Commissioner
1993 T.C. Memo. 196 (U.S. Tax Court, 1993)
St. Jude Medical v. Comm'r
97 T.C. No. 33 (U.S. Tax Court, 1991)

Cite This Page — Counsel Stack

Bluebook (online)
97 T.C. No. 33, 97 T.C. 457, 1991 U.S. Tax Ct. LEXIS 93, Counsel Stack Legal Research, https://law.counselstack.com/opinion/st-jude-medical-v-commr-tax-1991.