PDK Labs Inc. v. Reno

134 F. Supp. 2d 24, 2001 U.S. Dist. LEXIS 333, 2001 WL 273084
CourtDistrict Court, District of Columbia
DecidedJanuary 16, 2001
DocketCIV. A. 00-2894(HHK)
StatusPublished
Cited by15 cases

This text of 134 F. Supp. 2d 24 (PDK Labs Inc. v. Reno) is published on Counsel Stack Legal Research, covering District Court, District of Columbia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
PDK Labs Inc. v. Reno, 134 F. Supp. 2d 24, 2001 U.S. Dist. LEXIS 333, 2001 WL 273084 (D.D.C. 2001).

Opinion

MEMORANDUM OPINION AND ORDER

KENNEDY, District Judge. '

PDK Labs Inc. (“PDK”) is a New York corporation that manufactures over-the-counter pharmaceutical and vitamin products. Ephedrine is an ingredient that is used in the manufacture of these products. Unfortunately, ephedrine can also be used to produce illegal controlled substances, most notably methamphetamine, when extracted from lawful over-the-counter medicines. This process is known as “diversion.” Because of this possibility, the government classifies ephedrine as a List I chemical and regulates its importation into the United States. In October of *27 the year just ended, Indace, Inc., a company registered with the Drug Enforcement Administration to import List I chemicals, notified DEA of its intention to import three metric tons of ephedrine from India and that PDK was the purchaser of the ephedrine. The Drug Enforcement Administration blocked the importation of the ephedrine and continues to do so, an action which PDK claims is unlawful and is causing it irreparable injury.

PDK brings this case 1 against the Attorney General of the United States and the Administrator of the Drug Enforcement Administration, in their official capacities, as well as against the United States Department of Justice and the Drug Enforcement Administration (collectively “defendants” or “DEA”), seeking in-junctive and declaratory relief and a writ of mandamus. PDK maintains that DEA has (1) violated the Administrative Procedure Act (Counts I though IV); (2) deprived PDK of its property and liberty interests in violation of the Fifth Amendment’s due process clause (Count V); and (3) failed to perform its statutory duties (Count VI). Presently before the court is PDK’s motion for a preliminary injunction and defendant’s motion to dismiss. Upon consideration of the motions, the respective oppositions thereto, the oral arguments of counsel at a hearing and the testimony presented at that hearing, and the record in this case, the court concludes that each motion should be granted in part.

I. BACKGROUND

A. Importation Approval Process

Pursuant to section 6053 of the Chemical Diversion and Trafficking Act (“CDTA”), Pub.L. 100-690,102 Stat. 4181 (1988), codified as amended at 21 U.S.C. § 971, (“the statute” or “ § 971”), DEA regulates the importation of certain listed chemicals. Importers are required to notify DEA at least 15 days prior to the scheduled date of arrival of such chemicals. 21 U.S.C. § 971(a). Notification consists of the filing of an Import Declaration Form 486. 21 C.F.R. § 1313.12(b). Following notification, the statute and its implementing regulations permit DEA to issue a notice of suspension of importation based on evidence that the chemical may be diverted to the clandestine manufacture of controlled substances. A suspension order must contain the legal and factual basis for its issuance. 21 U.S.C. § 971(c)(1). After a suspension order has been issued the regulated person may not carry out the transaction. However, a regulated person to whom a suspension order applies has 30 days in which to request a hearing, and upon such request a hearing must be held within 45 days. 21 U.S.C. § 971(c)(2); 21 C.F.R. § 1313.52,1313.54.

Several countries, of which India is one, will not permit the export of listed chemicals until they have received a letter-of-non-objection (“LONO”) acknowledging that the importer’s government does not object to the shipment. The LONO is as an outgrowth of a 1994 international initiative among several nations, including the United States, and the International Narcotics Control Board (“INCB”), a UN-based entity. Subsequently, in addition to the formal regulations concerning suspension orders, DEA created a process enabling those importers who need a LONO to obtain one. If an importer needs a LONO for a particular transaction it files a *28 Form 486 importation request accompanied ,by a written request that a LONO issue.

Upon request for a LONO, DEA will either issue one, in which case the transaction continues normally, or will decline to do so because it perceives a threat of downstream diversion for illicit purposes. When a LONO is not issued, the importer is notified and provided three options. The importer can either (1) withdraw its request for a LONO and cancel its Form 486, or (2) take no action and in 30 days DEA will deem the request withdrawn, or (3) request in writing its desire to pursue the matter further, in which case a suspen- ' sion order is issued. If the importer elects option three, and a suspension order is issued, only then will DEA allow the importer the opportunity to obtain a hearing as provided for in § 971(c)(2). DEA maintains that the LONO process is standardized and consistent with the law; however, both parties recognize that it is not explicitly authorized in any statute or regulation.

B. Factual Allegations

On October 18, 2000, Indace, Inc., submitted a Form 486 notifying DEA of its intention to import three metric tons of ephedrine on November 14. The completed Form 486 specifically identified PDK as the purchaser of the ephedrine. On October 25, DEA informed Indace that a LONO would not be issued because there were grounds to believe the shipment would be diverted downstream for illegal uses, and notified Indace of the three courses it could pursue. 2

Indace informed DEA on November 1, that PDK planned to elect’ option three and pursue the matter further. Thereafter, on November 10, PDK wrote to DEA indicating that it was awaiting the issuance of a formal order of suspension. Indace then notified DEA on November 14, that it was not withdrawing its request because it was aware that PDK had elected to persist in its effort to obtain the ephedrine. In a November 17 telephone call with PDK’s counsel, and a subsequent November 22 letter, DEA expressed its position that under 21 U.S.C. § 971(c), PDK did not have standing to pursue this matter, and that therefore a suspension order could not be issued to PDK.

On December 4, PDK filed'this case. In light of DEA’s position, Indace notified DEA on December 5, that it regarded this matter as solely between “PDK' and DEA,” and that “Indace has no intent to exercise Option 3.” As a result on December 11, DEA notified Indace that since 30 days had passed after the denial of the LONO with no action by Indace, DEA considered the request for importation to be withdrawn.

II. LEGAL ANALYSIS

A. Defendants’ Rule 12(b)(1) Motion to Dismiss

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Bluebook (online)
134 F. Supp. 2d 24, 2001 U.S. Dist. LEXIS 333, 2001 WL 273084, Counsel Stack Legal Research, https://law.counselstack.com/opinion/pdk-labs-inc-v-reno-dcd-2001.