Burtman v. Garland

CourtDistrict Court, D. Arizona
DecidedMarch 28, 2024
Docket4:24-cv-00144
StatusUnknown

This text of Burtman v. Garland (Burtman v. Garland) is published on Counsel Stack Legal Research, covering District Court, D. Arizona primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Burtman v. Garland, (D. Ariz. 2024).

Opinion

1 WO 2 3 4 5 6 IN THE UNITED STATES DISTRICT COURT 7 FOR THE DISTRICT OF ARIZONA

9 Svetlana Burtman, No. CV-24-00144-TUC-SHR

10 Plaintiff, Order Denying Temporary Restraining Order 11 v.

12 Merrick Garland, et al.,

13 Defendants. 14 15 16 Pending before the Court is a Motion for Temporary Restraining Order (“TRO 17 Motion”) filed by Plaintiff Svetlana Burtman pursuant to Federal Rule of Civil Procedure 18 65. (Doc. 2.) Defendants filed a Response. (Doc. 10.) For the reasons stated below, the 19 Court denies the TRO Motion. 20 I. BACKGROUND 21 Plaintiff is a nurse practitioner who owns and operates two medical clinics—one is 22 in Tucson and the other is in Green Valley. (Doc. 1 at 2–3, 5.) Plaintiff is registered with 23 the DEA and was permitted to possess, prescribe, administer, and dispense controlled 24 substances. (Id. at 1.) 25 On July 19, 2023, the DEA investigated and audited Plaintiff’s Tucson Clinic. (Doc. 26 1 at 5; Doc. 1-2 at 4.) According to the Immediate Suspension order (“ISO”), 27 “[i]nvestigators were unable to complete their audit because of missing and incomplete 28 documentation as to inventory of controlled substances, purchase records, and dispensing 1 logs.” (Doc. 1-2 at 4.) The ISO alleges Plaintiff committed the following violations related 2 to the Tucson Clinic: 3 • clinic’s dispensing logs were incomplete and inconsistent • unable to provide complete records of your drug purchases 4 from at least two suppliers, Anazao Health Corporation and 5 Henry Schein • failed to conduct an initial inventory of all controlled 6 substances on hand when you first engaged in the 7 dispensing of controlled substances on November 27, 2017 • failed to conduct the required biennial inventories 8 • stored non-controlled substances with controlled 9 substances, without written authorization of the DEA Special Agent in charge 10 • failed to properly physically secure controlled substances 11 because controlled substances were found spread across different rooms of the clinic in unsecured cabinets 12 (Doc. 1-2 at 4.) 13 Also on July 19, 2023, the DEA visited Plaintiff’s Green Valley Clinic. The ISO 14 alleges the DEA visited this unregistered clinic to answer Plaintiff’s questions about 15 registration requirements. (Doc. 1-2 at 3.) According to the ISO, on September 20, 2023, 16 the DEA executed a warrant, collected logs/records, and discovered supplies of 17 testosterone at the unregistered Green Valley clinic. (Id. at 5.) The ISO alleges Plaintiff 18 lied to DEA investigators on July 19, 2023, when she denied ever having or dispensing 19 controlled substances at the Green Valley Clinic. (Id.) The ISO also alleges she “lied to 20 DEA investigators on September 23, 2023, when [she] claimed that the testosterone was 21 only on-site at the Green Valley Clinic because [she was] ‘prepping the office.’” (Id. at 5– 22 6.) 23 On December 28, 2023, the DEA issued the ISO, immediately suspending 24 Plaintiff’s registration based on the belief Plaintiff’s continued registration constituted an 25 imminent danger to the public health and safety. (Doc. 1-2 at 1, 6.) Specifically, the ISO 26 stated: 27 Despite being specifically warned against doing so, you have 28 unlawfully stored and dispensed controlled substances at an 1 unregistered location. You have done so as recently as September 20, 2023. Your ongoing storage and issuance of 2 controlled substances at the Green Valley clinic poses an 3 imminent danger. 4 (Doc. 1-2 at 6.) The ISO also stated: 5 It is also the Agency’s preliminary finding, based on the facts and circumstances described [in the ISO] and in light of the 6 rampant and deadly problem of prescription controlled 7 substance abuse, that [Plaintiff’s] continued registration during the pendency of these proceedings would constitute “an 8 imminent danger to the public health or safety” because of the 9 substantial likelihood of an imminent threat that death, serious bodily harm, or abuse of controlled substances will occur in the 10 absence of this suspension. 11 (Doc. 1-2 at 6.) 12 Plaintiff was served the order to show cause and the ISO on February 29, 2024. 13 (Doc. 10-2 at 2.) On March 7, 2024, Plaintiff’s counsel submitted a hearing request to the 14 Office of the Administrative Law Judges (ALJ) for review of the DEA’s suspension and 15 issuance of a final order. (Doc. 10-3 at 2.) The same day, Plaintiff’s counsel answered the 16 order to show cause and requested a hearing regarding the summary suspension. (Doc. 10- 17 4.) The DEA Office of Administrative Hearing ordered the parties to submit prehearing 18 statements and set a prehearing conference for April 4, 2024. (Doc. 10-5 at 3–4.) 19 On March 13, Plaintiff filed a complaint for declaratory and injunctive relief from 20 the ISO to prevent Defendants—the Attorney General, the Administrator of the DEA, and 21 the DEA—from enforcing the ISO against her because the DEA’s allegations fail to 22 establish imminent danger. (Doc. 1 at 3.) Plaintiff also seeks to have the Court dissolve 23 or set aside the ISO under 21 U.S.C. § 824 or 5 U.S.C. § 706. (Doc. 1 at 3, 7–11.) 24 Also on March 13, Plaintiff filed this TRO Motion seeking a Court order: (1) 25 “[r]estraining DEA from enforcing the [ISO] during the pendency of administrative 26 proceedings pertaining to [Plaintiff’s] registration and pending application,” and (2) 27 “[r]equiring DEA to immediately return any registrations, licenses, forms, and controlled 28 substances seized.” (Doc. 2 at 10.) Defendants filed a response arguing Plaintiff cannot 1 meet the standard for obtaining preliminary injunctive relief. (Doc. 10 at 15.) 2 II. LEGAL STANDARDS 3 A. Registration Requirements for Controlled Substances 4 The Controlled Substances Act (CSA) and its implementing regulations create 5 restrictions on the distribution of controlled substances. See 21 U.S.C. §§ 801–971; 21 6 C.F.R. §§ 1300–1321. Distributors and prescribers of controlled substances are required 7 to register with the Attorney General. See 21 U.S.C. § 823. The Attorney General may 8 suspend and revoke registrations but, normally, it must first serve upon the registrant an 9 order to show cause why the registration should not be denied, revoked, or suspended. 21 10 U.S.C. § 824(c). The registrant may then request a hearing in front of an ALJ. Id. 11 However, “[t]he Attorney General may, in his discretion, suspend any registration 12 simultaneously with the institution of proceedings . . . in cases where he finds that there is 13 an imminent danger to the public health or safety.” 21 U.S.C. § 824(d)(1). 14 Under § 824(d), “the phrase ‘imminent danger to the public health or safety’ means 15 that, due to the failure of the registrant to maintain effective controls against diversion or 16 otherwise comply with the obligations of a registrant . . . , there is a substantial likelihood 17 of an immediate threat that death, serious bodily harm, or abuse of a controlled substance 18 will occur in the absence of an immediate suspension of the registration.” 21 U.S.C. § 19 824(d)(2).

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Bluebook (online)
Burtman v. Garland, Counsel Stack Legal Research, https://law.counselstack.com/opinion/burtman-v-garland-azd-2024.